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                             232 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Abnormalities of chromosome 6 may play a crucial role in gastric cancinogenesis 1994
77 2 p. 172-
1 p.
artikel
2 Acquired chromosome changes in cholesteatoma Lo Curto, F
1994
77 2 p. 189-
1 p.
artikel
3 Acquired chromosome changes in non neoplastic solid tissues and their significance in the origin of tumors Casalone, R.
1994
77 2 p. 183-
1 p.
artikel
4 Allelic imbalance in paragangliomas is specific for chromosome 11, the site of the predisposing gene van Schothorst, E.M.
1994
77 2 p. 168-
1 p.
artikel
5 Allelic loss studies in Cowden's disease with breast carcinoma Longy, M.
1994
77 2 p. 169-
1 p.
artikel
6 Allelotype analysis of pediatric solid tumors embedded in paraffin using the highly polymorphic microsatellites Visser, M.
1994
77 2 p. 150-
1 p.
artikel
7 A long range map covering a homozygously deleted region in a small cell lung cancer (SCLC) derived cell line Veldhuis, Patrick M.J.F.
1994
77 2 p. 188-
1 p.
artikel
8 A major susceptibility locus to murine lung carcinogenesis maps on chromosome 6 Pierotti, M.A.
1994
77 2 p. 153-
1 p.
artikel
9 Amplification and deregulated expression of cyclin D1 in human tumors 1994
77 2 p. 154-
1 p.
artikel
10 Amplification and expression of the chromosome 11q13 genes EMS1 and CCND1 in lung cancer Marx, P.T.J.
1994
77 2 p. 173-
1 p.
artikel
11 Amplification of 20q13 locus in breast cancer: -Defining the minimal region Tanner, M.
1994
77 2 p. 158-
1 p.
artikel
12 Amplifications on chromosomes 7p, 9q and 12q in glioblastoma revealed by reverse chromosome painting Fischer, Ulrike
1994
77 2 p. 181-
1 p.
artikel
13 Analysis of a balanced translocation on chromosome 1p36 in a neuroblastoma patient van der Drift, Pauline
1994
77 2 p. 174-
1 p.
artikel
14 Analysis of the neurofibromatosis type 2 gene in schwannomas Bijlsma, Emilia K.
1994
77 2 p. 178-
1 p.
artikel
15 An improved procedure to quickly isolate and sequence the termini of DNA inserts of yeast artificial chromosomes Geurts, Jan M.W.
1994
77 2 p. 151-
1 p.
artikel
16 A physical map of the short arm of chromosome 11 involved in childhood solid tumours and the Beckwith-Wiedemann syndrome Redeker, E.
1994
77 2 p. 168-
1 p.
artikel
17 A single mutation in the RET proto-oncogene is associated with multiple endocrine neoplasia type 2B Hofstra, Robert M.W.
1994
77 2 p. 175-
1 p.
artikel
18 Association of 17p loss with late-stage or refractory disease in hematologic malignancy Hawkins, Jacqueline M.
1994
77 2 p. 134-143
10 p.
artikel
19 A synovial sarcoma with a complex (X;18;5;4) translocation and a break in the ornithine aminotransferase (OAT)Li cluster on Xp11.2 Olde Weghuis, D.
1994
77 2 p. 199-
1 p.
artikel
20 At least two different regions are involved in allelic imbalance on chromosome 16q in breast cancer Cleton-Jansen, Anne-Marie
1994
77 2 p. 169-
1 p.
artikel
21 A Wilms' tumour revisited: Complex abnormalities involving the short arm of chromosome 11 revealed by FISH Slater, R.M.
1994
77 2 p. 198-
1 p.
artikel
22 A yeast artificial chromosome (YAC) that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2 Suijkerbuijk, R.F.
1994
77 2 p. 176-
1 p.
artikel
23 Biochemical characterization of a product encoded by the EMS1 gene located in the chromosome 11q13 region and amplified in several breast, head and neck carcinomas 1994
77 2 p. 171-
1 p.
artikel
24 Breakpoint at band q13 on both chromosomes 12 in a paraosteal chondroma Verhest, A.
1994
77 2 p. 200-
1 p.
artikel
25 Characterisation of genes mapping in a region of 3p21 homozygously deleted in a small cell lung cancer (SCLC) derived cell line Kok, Klaas
1994
77 2 p. 187-
1 p.
artikel
26 Characteristic karyotypic features in non-squamous cell carcinomas of the head and neck Jin, Yuesheng
1994
77 2 p. 188-
1 p.
artikel
27 Characterization of a primary cell culture obtained from an adenomatous polyp in a patient with familial adenomatous polyposis (FAP) Grammatico, P.
1994
77 2 p. 171-
1 p.
artikel
28 Characterization of chromosome 12 anomalies in human germ cell tumors Suijkerbuijk, R.F.
1994
77 2 p. 160-
1 p.
artikel
29 Characterization of the chromosomal regions involved in the Beckwith-Wiedemann syndrome Alders, M.
1994
77 2 p. 168-
1 p.
artikel
30 Characterization of the translocation breakpoint region t(11;12) (q13;q12–q13) in the lipoma T92153 Merscher, S.
1994
77 2 p. 162-
1 p.
artikel
31 Chromosomal aberrations in four squamous cell carcinomas of the oral cavity Braun, S.
1994
77 2 p. 189-
1 p.
artikel
32 Chromosomal abnormalities and their prognostic value in human astroglial neoplasms 1994
77 2 p. 180-
1 p.
artikel
33 Chromosomal instability in patients with breast invasive ductal carcinomas (BIDC) 1994
77 2 p. 184-
1 p.
artikel
34 Chromosome abberations and DNA ploidy during malignant progresson of Barrett's esophagus Krishnadath, K.K.
1994
77 2 p. 188-
1 p.
artikel
35 Chromosome aberrations in a case of endometrial carcinoma Haus, Olga
1994
77 2 p. 197-
1 p.
artikel
36 Chromosome 1 aberrations in 34 breast cancer samples detected by a dual-target FISH technique 1994
77 2 p. 185-
1 p.
artikel
37 Chromosome aberrations in fibrous dysplasia Cin, Paola Dal
1994
77 2 p. 114-117
4 p.
artikel
38 Chromosome abnormalities in breast fibroadenomas Ozisik, Yavuz Y.
1994
77 2 p. 125-128
4 p.
artikel
39 Chromosome abnormalities in non small cell lung carcinoma Viguié, Franck
1994
77 2 p. 187-
1 p.
artikel
40 Chromosome 15 allelic imbalances and parental methylation status in germ cell tumors of the adult testis Looijenga, L.H.J.
1994
77 2 p. 152-
1 p.
artikel
41 Chromosome alterations in breast and colorectal adenocarcinomas: Same meaning? Dutrillaux, Bernard
1994
77 2 p. 157-
1 p.
artikel
42 Chromosome analysis of 73 thyroid neoplasms Roque, Lucia
1994
77 2 p. 190-
1 p.
artikel
43 Chromosome 3 and cancer Buys, Charles H.C.M.
1994
77 2 p. 159-
1 p.
artikel
44 Chromosome 12q13–q15 translocation breakpoints in solid tumors 1994
77 2 p. 161-
1 p.
artikel
45 Clinical studies of 40 cases of papillary bladder carcinomas; Cytogenetic, flow / image cytometry and FISH investigations 1994
77 2 p. 193-
1 p.
artikel
46 Clonal chromosome aberrations in fibroadenomas of the breast — Early signs indicating phyllodes tumors? Rohen, Corina
1994
77 2 p. 202-
1 p.
artikel
47 Clonal evolution in bone and soft tissue tumors 1994
77 2 p. 203-
1 p.
artikel
48 Clonality of combined testicular germ cell tumors of adults Gillis, A.J.M.
1994
77 2 p. 195-
1 p.
artikel
49 Clonal karyotypic abnormalities in colorectal adenomas: Clues to the early genetic events in the adenoma-carcinoma sequence Bomme, Lilian
1994
77 2 p. 186-
1 p.
artikel
50 Clonal karyotypic changes in benign epithelial hyperplasias of the breast 1994
77 2 p. 184-
1 p.
artikel
51 Cloning of a putative meningioma tumor suppressor gene Riegman, Peter H.J.
1994
77 2 p. 174-
1 p.
artikel
52 Coexpression analysis of c-Myc related genes NM23, Max, Mad, Mxi, c-fos, c-jun and c-myb in small cell lung cancer with high steady state c-Myc transcription Wundrack, Iris
1994
77 2 p. 173-
1 p.
artikel
53 Comparative genomic hybridization as a tool to define two distinct chromosome 12-derived amplification units in well-differentiated liposarcomas Suijkerbuijk, Ron F.
1994
77 2 p. 200-
1 p.
artikel
54 Comparative genomic hybridization: Methodology and application in the analysis of genetic aberrations in human solid tumors Kallioniemi, A.
1994
77 2 p. 149-
1 p.
artikel
55 Comparative genomic hybridization of uveal melanoma Prescher, Gabriele
1994
77 2 p. 163-
1 p.
artikel
56 Comparative study of a diffuse gastric cancer and its metastasis by cytogenetics, comparative genomic hybridization and southern blotting 1994
77 2 p. 172-
1 p.
artikel
57 Competitive genome hybridisation (CGH) analysis of numerical abnormalities in ovarian and breast cancer DNA 1994
77 2 p. 163-
1 p.
artikel
58 Conventional cytogenetics versus fluorescence in situ hybridisation for detailed karyotypic analysis of a small cell lung carcinoma cell line U2020 1994
77 2 p. 187-
1 p.
artikel
59 Cytogenetic aberrations of chromosome 12 in human solid tumors 1994
77 2 p. 160-
1 p.
artikel
60 Cytogenetic aberrations of chromosome 1p in embryonal rhabdomyosarcoma cell lines 1994
77 2 p. 201-
1 p.
artikel
61 Cytogenetically unrelated clones in pancreatic carcinomas Gorunova, Ludmila
1994
77 2 p. 190-
1 p.
artikel
62 Cytogenetical studies on oral squamous cell carcinoma Hermsen, M.
1994
77 2 p. 188-
1 p.
artikel
63 Cytogenetical study of a combined germ cell tumor of the testis van Echten, Jannie
1994
77 2 p. 195-
1 p.
artikel
64 Cytogenetic analisis of embryonal rhabdomyosarcoma Petković, Iskra
1994
77 2 p. 201-
1 p.
artikel
65 Cytogenetic analysis of adenocarcinomas of the lung Johansson, Maria
1994
77 2 p. 186-
1 p.
artikel
66 Cytogenetic analysis of prostate adenocarcinomas by interphase DNA in situ hybridization Alers, J.C.
1994
77 2 p. 194-
1 p.
artikel
67 Cytogenetic and fluorescence in situ hybridisation (FISH) analysis of ocular melanoma Beverstockl, Geoffrey C.
1994
77 2 p. 182-
1 p.
artikel
68 Cytogenetic and immunohistochemical characterization of a primary cell culture (KUM1) obtained from an urothelial carcinoma of the ureter Grammatico, P.
1994
77 2 p. 194-
1 p.
artikel
69 Cytogenetic characterization of different types of solid tumors in Saudis — First report 1994
77 2 p. 204-
1 p.
artikel
70 Cytogenetic characterization of renal cell carcinoma compared with clinical and histopathological data Junker, K.
1994
77 2 p. 193-
1 p.
artikel
71 Cytogenetic characterization of two cell lines obtained from ascites and ovarian adenocarcinoma of the same patient Dalprà, L.
1994
77 2 p. 197-
1 p.
artikel
72 Cytogenetic evidence for cell fusion during tumor progression of a nonseminomatous germ cell tumor of the testis 1994
77 2 p. 195-
1 p.
artikel
73 Cytogenetic evidence that carcinoma in situ is the precursor lesion for invasive testicular germ cell tumors van Echten, Jannie
1994
77 2 p. 194-
1 p.
artikel
74 Cytogenetic findings in 172 breast carcinomas — Identification of karyotypic subgroups 1994
77 2 p. 157-
1 p.
artikel
75 Cytogenetic findings in 152 colorectal adenocarcinomas — Correlation with clinicopathologic features 1994
77 2 p. 158-
1 p.
artikel
76 Cytogenetic investigation of five newly established cell lines from cervical cancer with G-banding and fluorescence in situ hybridisation (FISH), using chromosome-specific paint probes Thein, A.T.A.
1994
77 2 p. 197-
1 p.
artikel
77 Cytogenetic investigations of 127 benign thyroid hyperplasias and adenomas Belge, Gazanfer
1994
77 2 p. 190-
1 p.
artikel
78 Cytogenetics of 20 cases of genital carcinoma Couturier, Jérôme
1994
77 2 p. 196-
1 p.
artikel
79 Cytogenetics of fine needle aspirations of soft tissue tumors Molenaar, W.M.
1994
77 2 p. 203-
1 p.
artikel
80 Cytogenetics of renal oncocytomas Gunawan, B.
1994
77 2 p. 192-
1 p.
artikel
81 Cytogenetics of two cases of infantile yolk sac tumour Dijkhuizen, Trijnie
1994
77 2 p. 198-
1 p.
artikel
82 Cytogenetic studies in a chromophobe renal cell carcinoma Casadevall, C.
1994
77 2 p. 192-
1 p.
artikel
83 Cytogenetic studies of breast carcinomas Steinarsdóttir, Margrét
1994
77 2 p. 185-
1 p.
artikel
84 Cytogenetic study of a sporadic insulinoma 1994
77 2 p. 189-
1 p.
artikel
85 Cytogenetic study of renal cell carcinoma Aly, Maqdy S.
1994
77 2 p. 191-
1 p.
artikel
86 Cytogenetic survey of 48 Wilms' tumours Pantzar, Tapio
1994
77 2 p. 199-
1 p.
artikel
87 Defining the positions of the constitutive t(3,8) and t(3,6) breakpoints that occur in families with renal cell carcinoma van der Veen, Anneke
1994
77 2 p. 176-
1 p.
artikel
88 Deletion mapping in renal cell cancer adenoma and tumour tissue using chromosome 3-specific microsatellite makers Hulsbeek, Miriam
1994
77 2 p. 191-
1 p.
artikel
89 Deletion mapping of chromosomes 14, 8, 17, and 18 in 148 renal carcinomas with microsatellites (CA)n and correlation with clinicopathological features Fournet, J.C.
1994
77 2 p. 191-
1 p.
artikel
90 Detailed deletion mapping in renal cell carcinoma using chromosome 3-specific microsatellite markers van den Berg, Anke
1994
77 2 p. 191-
1 p.
artikel
91 Detection of aneuploidy for chromosome 1 by FISH in comparison with the general DNA content in (pre-)malignant cervical cancer Segets, P.
1994
77 2 p. 196-
1 p.
artikel
92 Detection of i (17 q) chromosome by fluorescent in situ hybridization (FISH) with interphase nuclei in medulloblastoma Vagner-capodano, A.M.
1994
77 2 p. 181-
1 p.
artikel
93 Detection of loss of heterozygosity in flow sorted ovarian tumor cells: Evidence for intra-tumor heterogeneity Abeln, Edwin C.A.
1994
77 2 p. 150-
1 p.
artikel
94 Detection of numerical alterations for chromosomes 7 and 12 in benign thyrid lesions by in situ hybridization. Histological implications 1994
77 2 p. 190-
1 p.
artikel
95 Detection of numeric and structural chromosome abnormalities in pediatric germ cell tumors by means of interphase cytogenetics 1994
77 2 p. 196-
1 p.
artikel
96 Detection of the episomal, linear, and integrated Epstein-Barr virus genome in human infected cells 1994
77 2 p. 167-
1 p.
artikel
97 Detection of trisomy of chromosome 8 in Ewing's sarcoma by fluorescence in situ hybridization 1994
77 2 p. 202-
1 p.
artikel
98 Different chromosomal evolution between embryonal and alveolar rhabdomyosarcoma during disease progression Niggli, F.K.
1994
77 2 p. 201-
1 p.
artikel
99 DNA amplification in human gliomas: A parallel study by modified CGH, FISH and Southern methods Almeida, Anna
1994
77 2 p. 156-
1 p.
artikel
100 DNA amplification in primary breast cancers with HSR(S) by a modified CGH technique Muleris, Martine
1994
77 2 p. 149-
1 p.
artikel
101 DNA analysis by image cytometry and corresponding cytogenetic investigations in urogenital carcinomas Sleegers, Eva
1994
77 2 p. 166-
1 p.
artikel
102 DNA fingerprint analysis in development and progression of human solid tumors Dahse, R.
1994
77 2 p. 183-
1 p.
artikel
103 Double-target FISH in the diagnosis of Ewing tumors Hattinger, Claudia M.
1994
77 2 p. 202-
1 p.
artikel
104 Double-target in situ hybridization in brightfield microscopy 1994
77 2 p. 165-
1 p.
artikel
105 Editorial comment: Fourth European Workshop Van Den Berghe, Herman
1994
77 2 p. 147-
1 p.
artikel
106 Elaboration of chromosome-detection kits based on non-isotopic in situ hybridization with chromosome-specific DNA probes for rapid analysis of chromosomal aberrations in human solid tumors Yurov, Yu.
1994
77 2 p. 165-
1 p.
artikel
107 Evaluation of cytogenetic changes in sporadic and familial neuroendocrine neoplasms Teijgeman, Ron
1994
77 2 p. 178-
1 p.
artikel
108 Evaluation of interphase fluorescence in situ hybridization (FISH) in DNA malignancy grading and comparison to static DNA cytometry in tumor cells Roitzheim, Barbara
1994
77 2 p. 166-
1 p.
artikel
109 Evidence for a gene on 17p13.3, distal to TP53, as a target for allele loss in breast tumors without p53 mutations Cornelis, R.S.
1994
77 2 p. 170-
1 p.
artikel
110 Expression of NM23H1 gene and monosomy of # 22 Simi, P.
1994
77 2 p. 177-
1 p.
artikel
111 Expression of the TLS/FUS and EWS genes in vitro and in vivo 1994
77 2 p. 155-
1 p.
artikel
112 Expression of the Wilms' tumour gene WT 1 in human malignant mesothelioma cell lines Langerak, Anthonie W.
1994
77 2 p. 203-
1 p.
artikel
113 Fine mapping of the human renal oncocytoma-associated t(5;11) chromosomal breakpoint in 11q13 Geurts van Kessel, A.
1994
77 2 p. 160-
1 p.
artikel
114 FISH analysis of derivative chromosome#3 in tumorigenic keratinocyte line 1994
77 2 p. 189-
1 p.
artikel
115 FISH and molecular analyses of chromosomal markers bearing genes amplification in adipose tissue tumors Pedeutour, F
1994
77 2 p. 162-
1 p.
artikel
116 FISH studies on ring and long-marker chromosomes from atypical lipomas and well-differentiated liposarcomas reveal involvement of region 12q13–q15 Kools, Patrick F.J.
1994
77 2 p. 161-
1 p.
artikel
117 Fluorescence in situ hybridization analysis using cosmid probes to define chromosome 6q abnormalities in ovarian carcinoma cell lines Lastowska, Maria A.
1994
77 2 p. 99-105
7 p.
artikel
118 Fluorescence in situ hybridization on cells isolated from lung brushes Hopman, A.
1994
77 2 p. 164-
1 p.
artikel
119 Further cytogenetic analysis of two testicular tumour cell lines with fluorescence in situ hybridisation (FISH) using chromosome specific paint probes, YACs and cosmids Wells, D.
1994
77 2 p. 195-
1 p.
artikel
120 Gene amplification and P1/P2 promoter shift as mechanisms of c-myc transcriptional activation in small cell lung cancer Dooley, Steven
1994
77 2 p. 155-
1 p.
artikel
121 Gene-identification with newly isolated CDNA clones covering the meningioma chromosomal region (MGCR) Janka, M.
1994
77 2 p. 179-
1 p.
artikel
122 Generation of antibodies against the neurofibromatosis type 2 gene product utilising the synthetic peptide strategy den Bakker, Michael A.
1994
77 2 p. 174-
1 p.
artikel
123 Genetic aberrations in bladder tumors detected by comparative genomic hybridization Voorter, C.
1994
77 2 p. 149-
1 p.
artikel
124 Genetic alterations in children with neuroblastoma (NBL) — Relevance to prognosis 1994
77 2 p. 179-
1 p.
artikel
125 Genetic alterations in high grade astrocytoma related to prognosis Leenstra, Sieger
1994
77 2 p. 181-
1 p.
artikel
126 Genetic analysis of a breast-ovarian cancer gene (BRCA1) on chromosome 17q Hamann, U.
1994
77 2 p. 154-
1 p.
artikel
127 Genetic elements in the multi-step lung carcinogenesis 1994
77 2 p. 159-
1 p.
artikel
128 Genetic heterogeneity in colonic carcinomas, adjacent adenomas and normal mucosa as detected with in situ hybridisation Herbergs, J.
1994
77 2 p. 158-
1 p.
artikel
129 Genome-wide survey of gains and losses of DNA sequences in primary prostate cancer by comparative genomic hybridization Visakorpi, T.
1994
77 2 p. 163-
1 p.
artikel
130 Genotype-phenotype correlation in APC familial and new mutation cases Gayther, Simon A.
1994
77 2 p. 171-
1 p.
artikel
131 Germline and somatic abnormalities of chromosome 7 in Wilms' tumor Wilmore, Helen P.
1994
77 2 p. 93-98
6 p.
artikel
132 Germline mutations in the von Hippel-Lindau tumor suppressor gene and preclinical diagnosis of gene carriers Brauch, Hiltrud
1994
77 2 p. 153-
1 p.
artikel
133 Glioma polyposis (Turcot syndrome): A case report of a rare hereditary disorder Maier-Hauff, K.
1994
77 2 p. 180-
1 p.
artikel
134 Hereditary renal cell carcinoma of papillary type Bernués, M.
1994
77 2 p. 192-
1 p.
artikel
135 Heterogeneity of astrocytomas evidenced by cytogenetics and in situ hybridization Bertrand, S.
1994
77 2 p. 181-
1 p.
artikel
136 Human malignant melanoma: Cytogenetic and immunohistochemical characterization on three primary cell cultures with t(1;14) Grammatico, P.
1994
77 2 p. 183-
1 p.
artikel
137 Human papillomavirus E6/E7 oncogenes and the P53 mediated response to DNA damage 1994
77 2 p. 178-
1 p.
artikel
138 Human testicular germ cell tumors show biallelic expression of the H19 and IGF2 gene 1994
77 2 p. 152-
1 p.
artikel
139 Identification of bcar-1, a putative breast cancer antiestrogen resistance locus by provirus insertion mutagenesis van Agthoven, Ton
1994
77 2 p. 185-
1 p.
artikel
140 Identification of genetic alterations and amplifications in neuroblastomas on the basis of chromosomal localization by competitive and comparative in situ hybridization Meddeb, M
1994
77 2 p. 180-
1 p.
artikel
141 Identification of two marker chromosomes in a human melanoma cell line by FISH Doneda, Luisa
1994
77 2 p. 182-
1 p.
artikel
142 Imprinting in development and disease 1994
77 2 p. 151-
1 p.
artikel
143 Improved fluorescence in situ hybridization technique for detection of apoptosis in paraffin embedded tumor tissue Lutz, Steffi
1994
77 2 p. 150-
1 p.
artikel
144 Increased gene expression of glutathion-S-transferase-pi in human lung carcinomas Verbeeck, MAE
1994
77 2 p. 173-
1 p.
artikel
145 In situ DNA methylation analysis of human tumor cells, mapping of methylcytosine rich bands Barbin, Agnès
1994
77 2 p. 150-
1 p.
artikel
146 In situ hybridization of two human somatostatin receptor genes (SSTR1 & 2) in breast carcinoma cell lines and allelic imbalance of these two genes in human primary breast tumours DeKlein, A.
1994
77 2 p. 185-
1 p.
artikel
147 Interphase cytogenetic investigations into hyperdiploidy in 11 cases of Wilms tumour — A comparison with classical cytogenetics and clinical outcome Fews, G.A.
1994
77 2 p. 198-
1 p.
artikel
148 Interphase spreading to study chromosome 11 p and q arm imbalances in bladder tumors by FISH 1994
77 2 p. 193-
1 p.
artikel
149 Investigation of the role of chromosome 18 in metastases of human solid tumours 1994
77 2 p. 177-
1 p.
artikel
150 In vitro cultivation, cytochemical and cytogenetic analysis of pediatric solid tumors Macek, M.
1994
77 2 p. 204-
1 p.
artikel
151 Involvement of the chromosome 11q13 region in human cancer Schuuring, Ed
1994
77 2 p. 155-
1 p.
artikel
152 Involvement of the chromosome 11q13 region in human cancer Schuuring, Ed
1994
77 2 p. 170-
1 p.
artikel
153 i(12p) in a testicular metastasis of renal cell carcinoma 1994
77 2 p. 192-
1 p.
artikel
154 Irregular overexpression of cyclin-d1 in cell lines with an 11q13 amplification, and by a tetracycline-responsive promotor Michalides, Rob
1994
77 2 p. 170-
1 p.
artikel
155 ISH and DNA ploidy analysis on paraffin sections of germ cell tumors Jenderny, J.
1994
77 2 p. 164-
1 p.
artikel
156 Isolation and mapping of DNA markers from the human 12q13–14 region by use of radiation hybrids and repeat element PCR 1994
77 2 p. 176-
1 p.
artikel
157 Isolation and regional assignment of chromosome 6 specific HNCDNA clones to analyze human malignant melanoma Meese, Eckart
1994
77 2 p. 182-
1 p.
artikel
158 Karyotypic heterogeneity in macroscopically distinct tumor areas in carcinomas of the breast 1994
77 2 p. 184-
1 p.
artikel
159 Karyotypic multiclonality in epithelial tumours Heim, Sverre
1994
77 2 p. 159-
1 p.
artikel
160 K-ras mutations as prognostic factor in human colorectal carcinomas Benhattar, Jean
1994
77 2 p. 155-
1 p.
artikel
161 Leukemia, lymphoma, and related disorders in families of children diagnosed with Wilms' tumor Hartley, Ann L.
1994
77 2 p. 129-133
5 p.
artikel
162 Linkage studies on hereditary nonpolyposis colorectal cancer in the Netherlands Wijnen, J.
1994
77 2 p. 171-
1 p.
artikel
163 Localization of 9p deletions in lung cancer Mead, L.J.
1994
77 2 p. 186-
1 p.
artikel
164 Loss of constitutional heterozygosity in a Beckwith Wiedemann Syndrome patient displaying a Wilms' tumour and nephrogenic rests Hoban, Paul R.
1994
77 2 p. 167-
1 p.
artikel
165 Loss of heterozygosity of chromosome 3 in subsets of uveal melanomas Sisley, Karen
1994
77 2 p. 183-
1 p.
artikel
166 Loss of the c-MET proto-oncogene from the deleted chromosome 7 of a uterine leiomyoma cell line Vanni, R.
1994
77 2 p. 203-
1 p.
artikel
167 Methodological development of fluorescence in situ hybridization Hyytinen, E.
1994
77 2 p. 164-
1 p.
artikel
168 Microdissection of chromosome 6q26–27 for the study of allele loss in ovarian cancer 1994
77 2 p. 164-
1 p.
artikel
169 Molecular analysis of chromosomal translocations in human extragonadal germ cell tumors Sinke, R.J.
1994
77 2 p. 176-
1 p.
artikel
170 Molecular analysis of the synovial sarcoma-specific t(X;18): Cloning of the breakpoint de Leeuw, B.
1994
77 2 p. 161-
1 p.
artikel
171 Molecular-cytogenetic analysis of centromeric breakpoints of chromosomal syndromes as effective approach to investigation of different human solid tumors Vorsanova, Svetlana G.
1994
77 2 p. 165-
1 p.
artikel
172 Molecular cytogenetic characterization of 1p deletions and 1;17 translocation breakpoints in neuroblastoma Van Roy, Nadine
1994
77 2 p. 157-
1 p.
artikel
173 Molecular cytogenetic study of soft tissue sarcoma 1994
77 2 p. 200-
1 p.
artikel
174 Molecular genetic studies of primary malignant liver tumours of childhood 1994
77 2 p. 154-
1 p.
artikel
175 Mouse models to identify genes involved in initiation and progression of tumorigenesis 1994
77 2 p. 152-
1 p.
artikel
176 Mutational activation of ras genes is absent in pediatric osteosarcoma 1994
77 2 p. 177-
1 p.
artikel
177 Mutations in the RET proto-oncogene in sporadic medullary thyroid carcinomas Stelwagen, Tineke
1994
77 2 p. 175-
1 p.
artikel
178 Neuroblastoma cells need normal cells for complete organogenic maturation Ambros, Inge M.
1994
77 2 p. 156-
1 p.
artikel
179 NF2 gene mutations in meningiomas and vestibular schwannomas Zwarthoff, Ellen C.
1994
77 2 p. 178-
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180 N-myc amplification in 241 neuroblastomas: Results of the german neuroblastoma study group Christiansen, H.
1994
77 2 p. 179-
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181 N-myc regulation in neuroblastoma Ngan Ching, Cheng
1994
77 2 p. 175-
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182 Non-radioactive detection and identification of p53 mutations in fixed and frozen tissues from human cancers 1994
77 2 p. 167-
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183 Nonrandom loss of human chromosome 3 fragments in scid tumors of mouse/human microcell hybrids. A potential method for tumor suppressor gene isolation? Imreh, S.
1994
77 2 p. 153-
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184 Nonrandom numerical aberrations of chromosomes 7, 9, and 10 in DNA-diploid bladder cancer Matsuyama, Hideyasu
1994
77 2 p. 118-124
7 p.
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185 No TP53 mutations in neuroblastomas detected by PCR-SSCP Castresana, Javier S.
1994
77 2 p. 180-
1 p.
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186 Numerical aberrations of chromosome 1 in relation to changes of DNA content in benign and malignant breast disease Verdoodt, B.
1994
77 2 p. 184-
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187 Numerical abnormalities of chromosomes 7, 17, 12, 16 and 20 in papillary kidney carcinomas detected by interphase cytogenetics in paraffin-embedded material 1994
77 2 p. 193-
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188 Oncogene amplifications in gastric carcinomas. A study of 27 primary tumors and 8 metastases 1994
77 2 p. 172-
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189 Oncogene and antioncogene from the 22q12 region involved in neuroectodermal tumours Thomas, G.
1994
77 2 p. 156-
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190 Pathogenesis of renal cell tumors: A cytogenetic model 1994
77 2 p. 160-
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191 1p deletion and gain of chromosome 12 in paraffin sections of an ovarian yolk sac tumor Meyer, A.
1994
77 2 p. 197-
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192 p53 gene mutation and protein accumulation in non small cell lung cancer do not predict survival 1994
77 2 p. 173-
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193 Physical mapping of chromosome 12q translocation breakpoints in one malignant and three benign solid tumors Schoenmakers, Eric F.P.M.
1994
77 2 p. 201-
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194 P53 mutations in thyroid tumors of the dog van Leeuwen, I.S.
1994
77 2 p. 169-
1 p.
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195 Prognostic value of chromosome anomalies in meningiomas — A study on 140 cases Henn, Wolfram
1994
77 2 p. 179-
1 p.
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196 Prostatic intraepithelial neoplasia (PIN) invasive carcinoma of the prostate: The same genetical entity? Szücs, S.
1994
77 2 p. 194-
1 p.
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197 12q13–14 amplica in human sarcomas without MDM2 include CDK4, SAS and GADD153/CHOP Forus, Anne
1994
77 2 p. 200-
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198 Rapid detection of APC mutations in FAP families and colorectal tumors by protein truncation test van der Luijt, R.B.
1994
77 2 p. 151-
1 p.
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199 Rearrangements of chromosomes 1 and 10 generate transforming fusion genes derived from TRK and RET tyrosine kinases in papillary thyroid carcinomas 1994
77 2 p. 175-
1 p.
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200 Reciprocal translocation t(12;13)(p13;q14) in acute nonlymphoblastic leukemia: Report and cytogenetic analysis of two cases Tosi, Sabrina
1994
77 2 p. 106-110
5 p.
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201 Recurrent 1;17 translocations in human neuroblastoma reveal non-homologous mitotic recombination during the S/G2 phase as a novel mechanism for LOH 1994
77 2 p. 156-
1 p.
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202 Refractory anemia with excess of blasts and isochromosome 12p in a patient with primary mediastinal germ-cell tumor Solé, F.
1994
77 2 p. 111-113
3 p.
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203 Regulation of p53 protein expression in human cancer Picksley, Steven M.
1994
77 2 p. 153-
1 p.
artikel
204 Retinoblastoma gene structure and product expression in human gastric carcinomas 1994
77 2 p. 172-
1 p.
artikel
205 Search for molecular alterations in Wilms' tumors Santos, AC
1994
77 2 p. 168-
1 p.
artikel
206 Sex chromosome conversion from XY to monosomy X to XX in brain tumor cells Hecht, Barbara K.
1994
77 2 p. 157-
1 p.
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207 Spectrum of somatic APC mutation in sporadic and inherited colorectal cancer Gupta, Sioban Sen
1994
77 2 p. 186-
1 p.
artikel
208 Strand-specific FISH: A new method for analysis of pericentromeric heterochromatin in mammalian chromosomes 1994
77 2 p. 149-
1 p.
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209 Structural characterization of a c-myc amplicon in a human lung cancer cell line Holzmann, Karlheinz
1994
77 2 p. 187-
1 p.
artikel
210 Studies of allelic imbalance on chromosome 1 in breast cancer 1994
77 2 p. 170-
1 p.
artikel
211 Studies on the involvement of chromosome 12 in Wilm's tumour Mitchell, Erika L.D.
1994
77 2 p. 198-
1 p.
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212 Study of numerical chromosome aberrations in prostate cancer, using FISH 1994
77 2 p. 159-
1 p.
artikel
213 Sub-chromosomal localization of a putative tumor-suppressor gene involved in cervical cancers to 11q22–q24 Hampton, G.M.
1994
77 2 p. 196-
1 p.
artikel
214 Suppression of EWS/FLI-1 oncogene function by transient transfection of dominant negative acting recombinant derivatives Kovar, H.
1994
77 2 p. 154-
1 p.
artikel
215 The canine karyotype: A trap for telomeric associations? Reimann, Nicola
1994
77 2 p. 169-
1 p.
artikel
216 The Fourth European Workshop on Cytogenetics and Molecular Genetics of Human Solid Tumors 1994
77 2 p. 148-
1 p.
artikel
217 The genetics of colorectal cancer 1994
77 2 p. 151-
1 p.
artikel
218 The multiple endocrine neoplasia type 2 syndromes and Hirschsprung disease are due to different mutations in the receptor tyrosine kinase ret Ponder, Bruce
1994
77 2 p. 158-
1 p.
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219 The Resource for Molecular Cytogenetics at the Lawrence Berkeley Laboratory and the University of California, San Francisco Weier, Heinz-Ulrich
1994
77 2 p. 165-
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220 The t(X;18) found in synovial sarcoma involves two distinct loci on the X chromosome Shipley, Janet
1994
77 2 p. 199-
1 p.
artikel
221 The use of fluorescence in situ hybridization (FISH) to measure initial and radiation induced chromosome aberrations in solid tumors Coco-Martin, Jose M.
1994
77 2 p. 166-
1 p.
artikel
222 The use of fluorescence in situ hybridization (FISH) to predict radiosensitivity of human tumor cell lines Coco-Martin, Jose M.
1994
77 2 p. 166-
1 p.
artikel
223 Toward the gene(s) for Wiedemann-Beckwith syndrome and associated tumors in 11p15 Henry, I.
1994
77 2 p. 152-
1 p.
artikel
224 TP53 mutations in malignant tumors in neurofibromatosis type 1 1994
77 2 p. 174-
1 p.
artikel
225 Translocation (9;22) (q34;q12–13) in a case of childhood rhabdoid tumor Heimann, P.
1994
77 2 p. 202-
1 p.
artikel
226 Two categories of synovial sarcoma defined by t(X;18) breakpoints on chromosome Xp Knight, Jennifer C.
1994
77 2 p. 161-
1 p.
artikel
227 Two distinct X chromosome breakpoints in t(X;18)-positive synovial sarcomas de Leeuw, B.
1994
77 2 p. 199-
1 p.
artikel
228 Two subclones in a case of uveal melanoma Prescher, Gabriele
1994
77 2 p. 144-146
3 p.
artikel
229 Two variants of the TLS-CHOP fusion transcript in myxoid liposarcomas with the 12;16 translocation Panagopoulos, Ioannis
1994
77 2 p. 177-
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230 Use of karyotyping, FISH and CGH for characterization of genome imbalances in tumor cells Giollant, M.
1994
77 2 p. 163-
1 p.
artikel
231 Visualization of chromosomal subregions in normal and neoplastic cells by PCR-mediated in situ hybridization methods Krijtenburg, P.J.
1994
77 2 p. 167-
1 p.
artikel
232 Xenograpted medulloblastomas: Cytogenetic and FISH analysis Vénuat, AM
1994
77 2 p. 182-
1 p.
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                             232 gevonden resultaten
 
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