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                             25 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Acute promyelocytic leukemia with t(15;16;17;19) and unusual fluorescence in situ hybridization pattern with PML and RARA probes Kamal, Nazmi Ragheb
1996
92 1 p. 54-57
4 p.
artikel
2 Announcement 1996
92 1 p. 94-
1 p.
artikel
3 A singular case of near-haploid stemline karyotype in a renal oncocytoma Gregori-Romero, M.Aurelia
1996
92 1 p. 28-30
3 p.
artikel
4 Chromosome 14 alteration is associated with increased collagenase expression and the metastatic potential of murine melanomas Dave, Bhavana J.
1996
92 1 p. 66-72
7 p.
artikel
5 Clonal chromosome changes including a del(6q) in a possible early lymphoma Atkin, N.B.
1996
92 1 p. 87-89
3 p.
artikel
6 Cytogenetic and clinicobiological features of acute leukemia with stem cell phenotype: Study of nine cases Cuneo, Antonio
1996
92 1 p. 31-36
6 p.
artikel
7 Cytogenetic study of neuroendocrine carcinoma of Merkel cells Vázquez-Mazariego, Y
1996
92 1 p. 79-81
3 p.
artikel
8 Development of minimally differentiated acute myeloblastic leukemia with novel isochromosome 18p and antecedent aplastic anemia Keung, Yi-Kong
1996
92 1 p. 1-3
3 p.
artikel
9 Dichotomy of hyperdiploid acute lymphoblastic leukemia on the basis of the distribution of gained chromosomes Mertens, Fredrik
1996
92 1 p. 8-10
3 p.
artikel
10 Editorial Board 1996
92 1 p. IFC-
1 p.
artikel
11 Isochromosome 14q in T cell childhood acute lymphoblastic leukemia Silva, Maria Luiza M.
1996
92 1 p. 92-93
2 p.
artikel
12 Klinefelter syndrome and neoplasia presentation of three new cases Wysocka, Barbara
1996
92 1 p. 85-86
2 p.
artikel
13 Linkage and cytogenetic mapping of a CAG repeat containing human cDNA to 3p24.2-p22 Polymeropoulos, Mihael H.
1996
92 1 p. 46-49
4 p.
artikel
14 Loss of heterozygosity on chromosome 22 in human gliomas does not inactivate the neurofibromatosis type 2 gene Watkins, David
1996
92 1 p. 73-78
6 p.
artikel
15 Molecular genetics and cytogenetics of breast carcinomas: Comparison of the two methods Valgardsdottir, Rut
1996
92 1 p. 37-42
6 p.
artikel
16 Selection of probes for fluorescence in situ hybridization analysis by differential display polymerase chain reaction of mRNA from rhabdomyosarcoma Pienkowska, Malgorzata
1996
92 1 p. 58-65
8 p.
artikel
17 Structural abnormalities of chromosome 7q in chronic lymphoproliferative disorders Oscier, D.G.
1996
92 1 p. 24-27
4 p.
artikel
18 Tandem triplication and quadruplication of chromosome 21 in childhood acute lymphoblastic leukemia Baialardo, Edgardo M.
1996
92 1 p. 43-45
3 p.
artikel
19 Telomere associations in desmoplastic infantile ganglioglioma Park, Jonathan P.
1996
92 1 p. 4-7
4 p.
artikel
20 Tetraploid or near-tetraploid clones characterized by two 8;21 translocations and other chromosomal abnormalities in two patients with acute myeloblastic leukemia Yongquan Xue,
1996
92 1 p. 18-23
6 p.
artikel
21 The accumulation and occurrence of clonal and unstable rearrangements are independent in colorectal cancer cells Muleris, Martine
1996
92 1 p. 11-13
3 p.
artikel
22 The detection of trisomies 8 and 9 in patients with essential thrombocytosis by fluorescence in situ hybridization Elis, A.
1996
92 1 p. 14-17
4 p.
artikel
23 Translocation (2;3)(p21;p26) as the sole anomaly in a benign localized fibrous mesothelioma Mertens, Fredrik
1996
92 1 p. 90-91
2 p.
artikel
24 Translocation (6;9;22)(p25;q34;q11.2) identified by FISH in acute leukemia González, G.J.R.
1996
92 1 p. 82-84
3 p.
artikel
25 Translocation t(15;17) in acute myelogenous leukemia with atypical megakaryoblastic features: Diagnostic, clinical, and therapeutic implications Morgan, David L.
1996
92 1 p. 50-53
4 p.
artikel
                             25 gevonden resultaten
 
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