Digitale Bibliotheek
Sluiten Bladeren door artikelen uit een tijdschrift
 
Zoeken naar met titel:
ABCDEFGHIJKLMNOPQRSTUVWXYZ

     Tijdschrift beschrijving
       Alle jaargangen van het bijbehorende tijdschrift
         Alle afleveringen van het bijbehorende jaargang
                                       Alle artikelen van de bijbehorende aflevering
 
                             182 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Abberations in E-cadherin in lobular breast cancer Cleton-Jansen, A.M.
 1996
 91 2 p. 128-
1 p.
 artikel
2 Additional human SSX genes not involved in the t (X;18) (p11.2; p11.2) and molecular diagnosis of synovial sarcomas de Leuuw, B.
 1996
 91 2 p. 152-
1 p.
 artikel
3 A gene dosage effect is responsible for overexpression of the MUC1 gene in human breast cancer Bièche, I.
 1996
 91 2 p. 129-
1 p.
 artikel
4 A homozygous deletion at FRA3B in a lung adenocarcinoma cell line with normal expression of the FHIT gene Draaijers, Tineke G.
 1996
 91 2 p. 170-
1 p.
 artikel
5 Alteration of signal transduction by chromosomal rearrangements in papillary thyroid carcinoma Pierotti, M.A.
 1996
 91 2 p. 109-
1 p.
 artikel
6 A major role for a 3P21 region and lack of involvement of the t(3;8) breakpoint region in the development of renal cell carcinoma suggested by loss of heterozygosity analysis Veldhuis, P.M.J.F.
 1996
 91 2 p. 142-
1 p.
 artikel
7 Analysis of a constitutional balanced translocation T(1;17)(p36;q 11.2-12.1) in a neuroblastoma patient Van der Drift, P.
 1996
 91 2 p. 171-
1 p.
 artikel
8 Analysis of chromosome 1-rearrangements in endometrial carcinomas by comparative genomic hybridization and loss of heterozygosity Hauspie, I.
 1996
 91 2 p. 137-
1 p.
 artikel
9 Analysis of primary and recurrent meningioma by combined cytogenetic techniques Dos Santos, S.E.
 1996
 91 2 p. 187-
1 p.
 artikel
10 An investigation of genetic alterations in gastric cancer Sud, R.
 1996
 91 2 p. 118-
1 p.
 artikel
11 A novel germline P53 insertion/duplication mutation in intron 6 in a Li-Frameni family Barel, D.
 1996
 91 2 p. 115-
1 p.
 artikel
12 A rapid genetic analysis of breast tumour samples using fish on FNA's Stevenson, D.A.J.
 1996
 91 2 p. 126-
1 p.
 artikel
13 A VNTR-sequence at 1P36 frequently deleted in solid tumours is amplified during normal differentiation Ambros, P.F.
 1996
 91 2 p. 175-
1 p.
 artikel
14 Biochemistry of mismatch recognition and its relevance to genomic instability Jiricny, J.
 1996
 91 2 p. 109-
1 p.
 artikel
15 Biphenotypic leukemia with a new translocation, t(2;6)(q31;q23) Taguchi, Hirokuni
 1996
 91 2 p. 104-105
2 p.
 artikel
16 BRCA 1 germline mutational spectrum in 21 Italian families Caligo, M.A.
 1996
 91 2 p. 112-
1 p.
 artikel
17 Cell cultivation and cytogenetic analysis of solid pediatric and adult bone tumors Macek, M.
 1996
 91 2 p. 155-
1 p.
 artikel
18 Cell-cycle regulators in lung cancer Marchetti, A.
 1996
 91 2 p. 165-
1 p.
 artikel
19 Cellular distribution of trisomies 8 and 12 in Ewing's sarcoma Maurici, D.
 1996
 91 2 p. 163-
1 p.
 artikel
20 CGH analysis of human breast tumors with known sets of amplications Courjal, F.
 1996
 91 2 p. 126-
1 p.
 artikel
21 Characterisation of a novel amplicon at 1q21-q22 in human sarcomas by CGH and molecular analysis Forus, A.
 1996
 91 2 p. 156-
1 p.
 artikel
22 Characterization of a region homozygously deleted in a small cell lung cancer cell line Timmer, T.
 1996
 91 2 p. 170-
1 p.
 artikel
23 Chop in liposarcoma, variations on a theme Aman, P.
 1996
 91 2 p. 147-
1 p.
 artikel
24 Chromosomal aberrations in ewing tumors: An evaluation by conventional cytogenetics and in situ hybridization techniques Hattinger, C.M.
 1996
 91 2 p. 162-
1 p.
 artikel
25 Chromosomal abnormalities in haemangiopericytomas Weibolt, V.M.
 1996
 91 2 p. 153-
1 p.
 artikel
26 Chromosomal analysis in non-myxoid and dedifferentiated myxoid liposarcomas Plaat, B.E.Ch.
 1996
 91 2 p. 146-
1 p.
 artikel
27 Chromosomal markers bearing chromosome 12 gene amplifications in adipose tissue tumours: Fish, molecular analyses and immunohistochemistry of 18 tumours Pedeutour, F.
 1996
 91 2 p. 149-
1 p.
 artikel
28 Chromosomal markers bearing chromosome 12 gene amplifications in adipose tissue tumours: Fish, molecular analyses and immunohistochemistry of 18 tumours Pedeutour, F.
 1996
 91 2 p. 148-
1 p.
 artikel
29 Chromosome 9 aberrations in laryngeal carcinoma: A cytogenetic and molecular study of seven cases Maggi, F.
 1996
 91 2 p. 177-
1 p.
 artikel
30 Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families Petersson, C.
 1996
 91 2 p. 124-
1 p.
 artikel
31 Chromosome aberrations in two osteosarcoma Petkovic, I.
 1996
 91 2 p. 158-
1 p.
 artikel
32 Chromosome abnormalities and NM23-H1 expression in human renal carcinoma Andreani, G.
 1996
 91 2 p. 140-
1 p.
 artikel
33 Chromosome abnormalities in a patient with acute myeloid leukemia following mediastinal germ cell tumor Scaravaglio, P.
 1996
 91 2 p. 175-
1 p.
 artikel
34 Chromosome abnormalities in pediatric gliomas Bossolasco, P.
 1996
 91 2 p. 173-
1 p.
 artikel
35 Chromosome breakpoints distribution in non-melanoma skin cancer Pavarino, E.C.
 1996
 91 2 p. 179-
1 p.
 artikel
36 Chromosome 9q deletions in bladder cancer: Comparison of in situ hybridization and loss of heterozygosity van Tilborg, A.A.G
 1996
 91 2 p. 143-
1 p.
 artikel
37 Clinical impact of solid tumor cytogenetics Mitelman, F.
 1996
 91 2 p. 110-
1 p.
 artikel
38 Clonal chromosome aberrations accumulate with age in upper aerodigestive tract mucosa Jin, C.
 1996
 91 2 p. 166-
1 p.
 artikel
39 Comparative genomic hybridization analysis of wilms tumors Steenman, M.
 1996
 91 2 p. 142-
1 p.
 artikel
40 Comparative genomic hybridization and representational difference analysis as tools to identify and molecularly clone tumor-specific chromosomal anomalies Simons, A.
 1996
 91 2 p. 156-
1 p.
 artikel
41 Confining the breakpoint regions for the papillary renal cell carcinoma-associated t(X;1) (p 11;q21) Weterman, M.A.J.
 1996
 91 2 p. 138-
1 p.
 artikel
42 Contribution of cytogenetic and fish analysis to the diagnostic and prognosis of brain tumors 1996
 91 2 p. 173-
1 p.
 artikel
43 Correlations of APC mutation sites with number of colorectal polyps and retinal lesions Curia, M.C.
 1996
 91 2 p. 112-
1 p.
 artikel
44 Cytogenetic aberrations in mixed-lineage tumors of the breast Dietrich, C.
 1996
 91 2 p. 128-
1 p.
 artikel
45 Cytogenetic analysis in a series of soft tissue leiomyosarcomas Celli, P.
 1996
 91 2 p. 153-
1 p.
 artikel
46 Cytogenetic analysis of a rectal tumour from a member of a Li Fraumeni family Mitchell, E.L.D.
 1996
 91 2 p. 121-
1 p.
 artikel
47 Cytogenetic analysis of exocrine pancreatic carcinomas: Intratumor heterogeneity and nonrandom pattern of chromosome aberrations Gorunova, L.
 1996
 91 2 p. 119-
1 p.
 artikel
48 Cytogenetic and DNA analysis of chromophobe renal cell carcinoma Iqbal, M.A.
 1996
 91 2 p. 138-
1 p.
 artikel
49 Cytogenetic and fish studies in an anaplastic thyroid carcinoma Roque, L.
 1996
 91 2 p. 184-
1 p.
 artikel
50 Cytogenetic and fish study in 120 cases of prostate adenocarcinoma Qi, H.
 1996
 91 2 p. 144-
1 p.
 artikel
51 Cytogenetic and molecular abnormalities of 6q26-27 region characterize benign surface epithelial ovarian tumors Tibiletti, M.G.
 1996
 91 2 p. 133-
1 p.
 artikel
52 Cytogenetic and molecular genetic analysis of primary tumours and cell lines indicate that mutation or deletion of the MTS-1 gene is a rare event in uveal melanoma de Klein, A.
 1996
 91 2 p. 180-
1 p.
 artikel
53 Cytogenetic characterization of a clivus chordoma in a cancer family patient Malgara, R.
 1996
 91 2 p. 152-
1 p.
 artikel
54 Cytogenetic comparisons of colorectal metalpastic polyps, adenomas, and carcinomas: Karyotypic evidence for a common clonal origin in some patients Bardi, G.
 1996
 91 2 p. 120-
1 p.
 artikel
55 Cytogenetic findings in pituitary adenomas Bettio, D.
 1996
 91 2 p. 183-
1 p.
 artikel
56 Cytogenetic findings in 34 primary NSCLCS D'Alessandro, E.
 1996
 91 2 p. 168-
1 p.
 artikel
57 Cytogenetic findings on multiple leiomyosarcomas from the same patient Riva, P.
 1996
 91 2 p. 154-
1 p.
 artikel
58 Cytogenetic investigation of synchronous bilateral renal tumors Dal Cin, P.
 1996
 91 2 p. 142-
1 p.
 artikel
59 Cytogenetic investigations of 334 benign thyroid hyperplasias and adenomas Belge, G.
 1996
 91 2 p. 184-
1 p.
 artikel
60 Cytogenetic, molecular genetic and flow cytometry analysis of breast carcinomas: Association with TP53 abnormalities? Valgardsdóttir, R.
 1996
 91 2 p. 129-
1 p.
 artikel
61 Cytogenetics of borderline malignant soft tissue tumors: An aid for the histopathological diagnosis Molenaar, W.M.
 1996
 91 2 p. 154-
1 p.
 artikel
62 Cytogenetics revealing the diagnosis in metastases of unknown origin Dal Cin, P.
 1996
 91 2 p. 182-
1 p.
 artikel
63 Deletion mapping of long arm of chromosome 6 in gastric carcinoma Carvalho, B.
 1996
 91 2 p. 118-
1 p.
 artikel
64 Deletions of 3p in breast tumors Pandis, N.
 1996
 91 2 p. 125-
1 p.
 artikel
65 Detection and identification of mutations in the APC gene in portuguese fap families using the protein truncation test and SSCP Marshall, B.
 1996
 91 2 p. 113-
1 p.
 artikel
66 Detection of a fusion transcript between HMGI-C and the mitochondrial aldehyde dehydrogenase gene in a uterine leiomyoma with normal kartotype Kazmierczak, B.
 1996
 91 2 p. 136-
1 p.
 artikel
67 Detection of chromosome 3 abnormalities in cytospin and touch preparations of lung tumors using fluorescence in situ hybridization Varella-Garcia, M.
 1996
 91 2 p. 166-
1 p.
 artikel
68 Detection of chromosome copy number aberrations in osteosarcoma by fish Sarti, M.
 1996
 91 2 p. 158-
1 p.
 artikel
69 Detection of T(12;16) in myxoid liposarcomas and a myxoid sarcoma: Implication of the FUS/CHOP fusion in a broad spectrum of myxoid sarcomas Horsman, D.E.
 1996
 91 2 p. 147-
1 p.
 artikel
70 Determination of the amplicon structure of mammary carcinoma cell line MDA-MB-134 using fish de Leeuw, B.
 1996
 91 2 p. 124-
1 p.
 artikel
71 Determination of the smallest region of amplification in chromosomal band 17P12 in malignant astrocytomas Voesten, A.M.J.
 1996
 91 2 p. 172-
1 p.
 artikel
72 Different cytogenetic patterns in skeletal breast cancer metastases Adeyinka, A.
 1996
 91 2 p. 126-
1 p.
 artikel
73 Differential chromosome allelic imbalance in the progression of human prostate cancer Latil, A.
 1996
 91 2 p. 145-
1 p.
 artikel
74 Discontinuity of 12q13-22 amplicon in liposarcoma — microsatellite repeat analysis Wolf, M.
 1996
 91 2 p. 164-
1 p.
 artikel
75 Disseminated alveolar rhabdomyosarcoma with MYCN amplified HSR Jeison, M.
 1996
 91 2 p. 159-
1 p.
 artikel
76 DNA copy number changes in chondrosarcomas. Comparative genomic hybridization study Larramendy, M.L.
 1996
 91 2 p. 164-
1 p.
 artikel
77 Early involvement of 6q in epithelial ovarian tumors Bernasconi, B.
 1996
 91 2 p. 132-
1 p.
 artikel
78 Effect of interferon A and B in relation to differences in copy numbers of chromosomes 9 and 21 in four human melanoma cell lines Köpf, I.
 1996
 91 2 p. 181-
1 p.
 artikel
79 “Elimination test”: Solid tumor progression model based on the nonrandom changes of human chromosome 3 in monochromosomal microcell hybrid Imreh, S.
 1996
 91 2 p. 185-
1 p.
 artikel
80 Establishment of a 6 MB yac contig and long range physical map on human chromosome 12q15 encompassing the HMGI-C gene which is frequently rearranged in a variety of benign solid tumors Schoenmakers, E.F.P.M.
 1996
 91 2 p. 150-
1 p.
 artikel
81 Evaluation of cytogenetic abeerations occurring in multistep prostatic tumorigenesis by interphase in situ hybridization Alers, J.C.
 1996
 91 2 p. 144-
1 p.
 artikel
82 Evidence for complete mutational inactivation of the E-cadherin gene and loss of the wildtype protein in invasive lobular breast carcinoma Becker, I.
 1996
 91 2 p. 125-
1 p.
 artikel
83 EWS and FUS/TLS related genes Mencinger, M.
 1996
 91 2 p. 147-
1 p.
 artikel
84 Expression of the HMGI-C gene in uterine leiomyomas and myometrial tissues Rogalla, P.
 1996
 91 2 p. 135-
1 p.
 artikel
85 Failure to establish cell lines from uterine leiomyomas showing the DEL(7) as the sole abnormality Kazmierczak, B.
 1996
 91 2 p. 136-
1 p.
 artikel
86 Familial predisposition Ponder, B.A.J.
 1996
 91 2 p. 107-
1 p.
 artikel
87 Fifth European workshop on cytogenetics and molecular genetics of human solid tumors 1996
 91 2 p. 106-
1 p.
 artikel
88 Fish characterization of chromosome 19 rearrangements in glioma-derived cell lines Magnani, I.
 1996
 91 2 p. 172-
1 p.
 artikel
89 Fluorescence in situ hybridization on cells from urine and bladder washings in the diagnosis of bladder cancer Müller, C.
 1996
 91 2 p. 143-
1 p.
 artikel
90 Follicular thyroid carcinoma: Chromosome analysis of 19 cases Roque, L.
 1996
 91 2 p. 183-
1 p.
 artikel
91 Fusion of the EWS and CHOP genes in myxoid liposarcoma Panagopoulos, I.
 1996
 91 2 p. 146-
1 p.
 artikel
92 Gastric carcinoma in a female child with 18p- syndrome Haitink, O.
 1996
 91 2 p. 117-
1 p.
 artikel
93 Gene amplification and p53 expression in 123 bone and soft tissue sarcomas (BSTS) Peydró-Mellquist, A.
 1996
 91 2 p. 155-
1 p.
 artikel
94 Gene amplification and TP53 mutations in an experimental model of colorectal cancer Michel, P.
 1996
 91 2 p. 123-
1 p.
 artikel
95 Genetic alterations in human neuroblastoma and their clinical significance Schwab, M.
 1996
 91 2 p. 111-
1 p.
 artikel
96 Genetic analysis in the differential diagnosis of lipomatous tumor Peydró-Mellquist, A.
 1996
 91 2 p. 149-
1 p.
 artikel
97 Genetic analysis in the differential diagnosis of lipomatous tumors Peydró-Mellquist, A.
 1996
 91 2 p. 148-
1 p.
 artikel
98 Genetic basis of benign mesenchymal tumour development Van de Ven, W.J.M.
 1996
 91 2 p. 110-
1 p.
 artikel
99 Genetic instability and clonal karyotypic abnormalities in osteosarcoma diagnosed as aneurysmal bone cyst Adami Vayego, S.
 1996
 91 2 p. 157-
1 p.
 artikel
100 Genetic instability in early gastric cancer Palmirotta, R.
 1996
 91 2 p. 119-
1 p.
 artikel
101 Germline TP53 mutations in Li-fraumeni and Li-Fraumeni-like families - an updated study of 34 families Varley, J.M.
 1996
 91 2 p. 115-
1 p.
 artikel
102 Hepatocarcinogenesis: A polygenic model of inherited predisposition to cancer Dragani, T.A.
 1996
 91 2 p. 116-
1 p.
 artikel
103 Hereditary disorders defective in nucleotide-excision repair: Clinical and molecular aspects Stefanini, M.
 1996
 91 2 p. 108-
1 p.
 artikel
104 Heterochromatic variability of chromosome 1,9 and 16 in 57 children with solid tumors and 64 controls Petkovic, I.
 1996
 91 2 p. 176-
1 p.
 artikel
105 High glycolosis despite the loss of hexokinase transcription unit in chromosome-10 monosomic human gliomas Oudard, S.
 1996
 91 2 p. 173-
1 p.
 artikel
106 High incidence of cytogenetic aberrations in a series of 60 pulmonary chondroid hamartomas Kazmierczak, B.
 1996
 91 2 p. 169-
1 p.
 artikel
107 Hox genes regulation in small-cell lung cancers Flagiello, D.
 1996
 91 2 p. 167-
1 p.
 artikel
108 Hunting for EWS-FLI1 targets in Ewing tumors Mossier, B.
 1996
 91 2 p. 162-
1 p.
 artikel
109 Identification of marker chromosomes in three breast carcinoma cell lines by fish (reverse painting) Morris, J.S.
 1996
 91 2 p. 130-
1 p.
 artikel
110 Image analysis for fluorescence microscopy: An application to CGH Courjal, F.
 1996
 91 2 p. 182-
1 p.
 artikel
111 Immunodetection of the synovial sarcoma-associated SYT and SSX proteins dos Santos, N.R.
 1996
 91 2 p. 152-
1 p.
 artikel
112 Incidence of hereditary nonpolyposis colorectal cancer syndrome (HNPCC) in the U.S.S.L. N.3 and N.4 areas of lombardy region - preliminary report on epidemiological results Cornaggia, M.
 1996
 91 2 p. 114-
1 p.
 artikel
113 Incidence of other neoplasia in Italian melanoma-prone families with P16 (GLY93TRP) mutation Ciotti, P.
 1996
 91 2 p. 116-
1 p.
 artikel
114 Increased frequency of chromosomal aberrations in peripheral blood lymphocytes of patients with breast carcinoma Koncar Mubrin, M.
 1996
 91 2 p. 127-
1 p.
 artikel
115 In situ fluorescence hybridization analysis of deletion of the long arm of chromosome 7 in a uterine leiomyoma derived cell line Vanni, R.
 1996
 91 2 p. 137-
1 p.
 artikel
116 Interphase cytogenetics of gastric adenocarcinomas Gargano, D.
 1996
 91 2 p. 118-
1 p.
 artikel
117 Investigation of TP53 gene mutation in the exons 5 and 7 through PCR-SSCP technique in bone lesions Adami Vayego, S.
 1996
 91 2 p. 156-
1 p.
 artikel
118 In vivo evidence of a neural histogenesis for ewing sarcoma Knezevich, S.R.
 1996
 91 2 p. 160-
1 p.
 artikel
119 Involvement of chromosome 6 in endometrial cancer Tibiletti, M.G.
 1996
 91 2 p. 132-
1 p.
 artikel
120 Involvement of the chromosome 11Q13 region in human cancer Schuuring, E.
 1996
 91 2 p. 130-
1 p.
 artikel
121 Involvement of translin, a protein associated with lymphoid chromosome translocations, in the specific t(2;13) translocation in alveolar rhabdomyosarcoma Chalk, J.G.
 1996
 91 2 p. 160-
1 p.
 artikel
122 Isochromosome 12p and maternal loss of 1p36 in a pediatric testicular germ cell tumor Stock, Cornelia
 1996
 91 2 p. 95-100
6 p.
 artikel
123 Karyotype, chromosome instability and other genomic alterations in epithelial cancers. Do they correlate? Dutrillaux, B.
 1996
 91 2 p. 108-
1 p.
 artikel
124 Karyotypic comparisons of multiple tumorous and macroscopically normal surrounding tissue samples from patients with breast cancer Teixeira, M.R.
 1996
 91 2 p. 124-
1 p.
 artikel
125 Lack of recognition of a mouse centromere by anti-centromere proteins Vig, Baldev K.
 1996
 91 2 p. 101-103
3 p.
 artikel
126 Localization and ordering of the human 3PK gene and five other human chromosome 3 markers. Attempt to establish the borders of the nonrandomly eliminated putative chromosome 3 tumor suppressor regions in mouse-human microcell hybrid derived SCID tumors Szeles, A.
 1996
 91 2 p. 186-
1 p.
 artikel
127 Loss of heterozygosity at 6Q in malignant salivary gland tumors Queimado, L.
 1996
 91 2 p. 168-
1 p.
 artikel
128 Loss of 1P material in colorectal adenomas: A combined cytogenetic and molecular genetic study Bomme, L.
 1996
 91 2 p. 122-
1 p.
 artikel
129 Mapping of amplification units containing MDM2, CDK4 and HMGIC Berner, J.M.
 1996
 91 2 p. 150-
1 p.
 artikel
130 Mapping of the chromosome 8Q12 region with respect to translocation breakpoints in pleomorphic adenoma of the salivary glands Kas, K.
 1996
 91 2 p. 165-
1 p.
 artikel
131 Micronuclei can contain amplified genes Ambros, I.M.
 1996
 91 2 p. 185-
1 p.
 artikel
132 Microsatellite alterations pathological aspects of breast cancer De Marchis, L.
 1996
 91 2 p. 131-
1 p.
 artikel
133 Microsatellite instability and mutation of the DNA mismatch repair gene HMLH1 in gastric cancer Keller, G.
 1996
 91 2 p. 114-
1 p.
 artikel
134 Microsatellite instability in gastric carcinogenesis Veiga, I.
 1996
 91 2 p. 117-
1 p.
 artikel
135 Mitogenic signal transduction by SH2/SH3 proteins Lanfrancone, L.
 1996
 91 2 p. 109-
1 p.
 artikel
136 Molecular analysis of chromosome 19 aberrations in pancreatic carcinomas: Deletion of 19p13.2 and overrepresentation of 19q13.1–13.2 Höglund, M.
 1996
 91 2 p. 120-
1 p.
 artikel
137 Molecular analysis of patients with multiple renal cell tumours suggests that 3P21 loss is a prerequisite for malignancy van den Berg, Anke
 1996
 91 2 p. 139-
1 p.
 artikel
138 Molecular and cytogenetic investigation of ocular melanoma McNamara, M.
 1996
 91 2 p. 179-
1 p.
 artikel
139 Molecular and cytogenetic investigation of the DCC gene in colorectal cancer Baharuddin, P.
 1996
 91 2 p. 121-
1 p.
 artikel
140 Molecular and immunohistochemical study of the P53 tumor suppressor gene in skin cancers Pavarino, E.C.
 1996
 91 2 p. 178-
1 p.
 artikel
141 Molecular characterisation of an 8P minichromosome that includes the site of a tumour suppressor gene Delhanty, J.D.A.
 1996
 91 2 p. 123-
1 p.
 artikel
142 Molecular characterization of the fusion transcript observed in an aggressive angiomyxoma with a 12Q14-15 aberration Wanschura, S.
 1996
 91 2 p. 151-
1 p.
 artikel
143 Molecular cytogenetic characterization of two novel variant translocations in Ewing's sarcoma-related tumors Minoletti, F.
 1996
 91 2 p. 163-
1 p.
 artikel
144 Molecular diagnosis of Ewing's tumor Delattre, O.
 1996
 91 2 p. 111-
1 p.
 artikel
145 Molecular genetic analysis of MYCN and DDX1 co-amplification in pediatric solid tumours Pandita, A.
 1996
 91 2 p. 176-
1 p.
 artikel
146 Molecular genetic changes in carcinoma of the uterine cervix Kersemaekers, A.M.F.
 1996
 91 2 p. 134-
1 p.
 artikel
147 Molecular genetics of hereditary nonpolyposis colorectal cancer; basic research with clinical applications Aaltonen, L.A.
 1996
 91 2 p. 107-
1 p.
 artikel
148 Mutational screening of the NF2 gene in sporadic tumors of the central nervous system Vitelli, F.
 1996
 91 2 p. 174-
1 p.
 artikel
149 Mutations of HMSH2 and HMLH1 in Italian HNPCC families Radice, P.
 1996
 91 2 p. 113-
1 p.
 artikel
150 Novel formation and amplification of the PAX7-FKHR fusion gene in a case of alveolar rhabdomyosarcoma Weber-Hall, S.
 1996
 91 2 p. 159-
1 p.
 artikel
151 Oncogene alterations in human bone tumors Gamberi, G.
 1996
 91 2 p. 157-
1 p.
 artikel
152 Origin and evolution of unbalanced karyotypes in XP fibroblast clones cultured in vitro Mondello, C.
 1996
 91 2 p. 181-
1 p.
 artikel
153 Ovarium germ cell tumor with chromosome 12 anomaly but without I(12P) Dal Cin, P.
 1996
 91 2 p. 135-
1 p.
 artikel
154 P53 alterations are predictive of aggressiveness in ovarian carcinomas Buttitta, F.
 1996
 91 2 p. 131-
1 p.
 artikel
155 p53 alterations in breast tumors in patients of Brazil Kvitko, K.
 1996
 91 2 p. 127-
1 p.
 artikel
156 Pathogenesis of renal cell tumors: A (cyto)-genetic model van den Berg, E.
 1996
 91 2 p. 141-
1 p.
 artikel
157 Patterns of oncogene activation in human neuroblastoma Corvi, R.
 1996
 91 2 p. 171-
1 p.
 artikel
158 P53 Mutations as a possible predictor of response to chemotherapy in metastatic colorectal cancers Benhattar, J.
 1996
 91 2 p. 122-
1 p.
 artikel
159 Rapid differential diagnosis for myxoid liposarcoma by fish on cytological preparations Mezzelani, A.
 1996
 91 2 p. 146-
1 p.
 artikel
160 RAS gene mutations in non-melanona skin cancers Rossit, A.R.B.
 1996
 91 2 p. 178-
1 p.
 artikel
161 Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization Marchio, A.
 1996
 91 2 p. 186-
1 p.
 artikel
162 Recurrent chromosome changes in trisomic 12 ovarian fibrothecomas Verhest, A.
 1996
 91 2 p. 134-
1 p.
 artikel
163 Secondary chromosome alterations in ocular melanomas and relationship to prognosis Sisley, K.
 1996
 91 2 p. 180-
1 p.
 artikel
164 Sensitive and efficient detection of MSH2 and MLH1 mutations in sporadic colon carcinomas by two-dimensional DNA electrophoresis Wu, Y.
 1996
 91 2 p. 121-
1 p.
 artikel
165 Similar patterns of gene expression in phenotypically variant tumours expressing the EWS/FLI1 gene fusion as assessed by differential display-PCR Lim, J.F.
 1996
 91 2 p. 161-
1 p.
 artikel
166 Simple method to obtain PCR products from paraffin embedded tissues after Bouin's solution fixation: Interests and limits Longy, M.
 1996
 91 2 p. 182-
1 p.
 artikel
167 Structural characterization, chromosomal localization and mutational analysis of the novel DNA-repair gene G/T glycosylase Sard, L.
 1996
 91 2 p. 167-
1 p.
 artikel
168 Telomerase activity and alterations of telomere length in renal cell carcinomas Dahse, R.
 1996
 91 2 p. 139-
1 p.
 artikel
169 The karyotyping of needle core biopsies in Wilms' tumour Betts, D.R.
 1996
 91 2 p. 143-
1 p.
 artikel
170 The NF2 tumor suppressor gene Thomas, G.
 1996
 91 2 p. 110-
1 p.
 artikel
171 The p21WAF1 gene is infrequently mutated in human ovarian tumours and p21WAF1 protein levels appear to be regulated independently of p53 status Milner, B.J.
 1996
 91 2 p. 133-
1 p.
 artikel
172 The role of 1P36.3 in pediatric germ cell tumors Stock, C.
 1996
 91 2 p. 174-
1 p.
 artikel
173 Tools for molecular cytogenetics Marzella, R.
 1996
 91 2 p. 187-
1 p.
 artikel
174 t(11;22)(q24;q12) in an extrarenal malignant rhabdoid tumor Mastik, M.F.
 1996
 91 2 p. 164-
1 p.
 artikel
175 Translocation t(17;22)(q21;q13) in dermatofibrosarcoma protuberans: A new tumour-associated rearrangement Pedeutour, F.
 1996
 91 2 p. 151-
1 p.
 artikel
176 Trisomy 8 and trisomy 20 in desmoid tumours Qi, H.
 1996
 91 2 p. 151-
1 p.
 artikel
177 Trisomy 6 in direct preparation of basal cell carcinoma (BBC) Casalone, R.
 1996
 91 2 p. 177-
1 p.
 artikel
178 Tumorgenetic investigations on metastasized renal cell carcinomas by cytogenetics; in-situ-hybridization and CGH Junker, K.
 1996
 91 2 p. 140-
1 p.
 artikel
179 Two cases of renal cell carcinoma, clear cell type, revealing a t(6;11)(p21;q13) Dijkhuizen, T.
 1996
 91 2 p. 141-
1 p.
 artikel
180 t(Y;22) in primary prostate tumors. A random or non random aberration? A combined G-banding and fish analysis Szücs, S.
 1996
 91 2 p. 145-
1 p.
 artikel
181 Warthin tumor: A cytogenetic study of 12 cases Martins, C.
 1996
 91 2 p. 169-
1 p.
 artikel
182 Why are P53 alterations preferentially found in cell lines? A functional study in the ewing tumor model Kovar, H.
 1996
 91 2 p. 161-
1 p.
 artikel
                             182 gevonden resultaten
 
 Koninklijke Bibliotheek - Nationale Bibliotheek van Nederland