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                             25 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Amplification of the MLL Region in Acute Myeloid Leukemia Park, Jonathan P
2000
121 2 p. 198-205
8 p.
artikel
2 A Novel Dicentric Deleted Chromosome 21 Arising from Tandem Translocation Robinson, L
2000
121 2 p. 208-211
4 p.
artikel
3 A Novel High Mobility Group Protein Gene Is a Candidate for Xp22 Abnormalities in Uterine Leiomyomas and Other Benign Tumors Blank, Cornelia
2000
121 2 p. 172-180
9 p.
artikel
4 Comparative Genomic Hybridization Reveals Recurrent Enhancements on Chromosome 20 and in One Case Combined Amplification Sites on 15q24q26 and 20p11p12 in Glioblastomas Brunner, Christian
2000
121 2 p. 124-127
4 p.
artikel
5 Concomitant Amplif ication and Expression of PAX7-FKHR and MYCN in a Human Rhabdomyosarcoma Cell Line Carrying a Cryptic t(1;13)(p36;q14) Frascella, Emanuela
2000
121 2 p. 139-145
7 p.
artikel
6 Cytogenetic and Fluorescence In Situ Hybridization Studies in Four Cases of Plasma Cell Leukemia Lloveras, Elisabet
2000
121 2 p. 163-166
4 p.
artikel
7 Deletion of 3′-CBFB Gene in Association with an Inversion (16)(p13q22) and a Loss of the Y Chromosome in a 2-Year-Old Child with Acute Myelogenous Leukemia-M4 Batanian, Jacqueline R
2000
121 2 p. 216-219
4 p.
artikel
8 Dicentric (17;18) in a Case of Atypical B-Cell Chronic Lymphocytic Leukemia Espinet, Blanca
2000
121 2 p. 194-197
4 p.
artikel
9 Establishment of a Human Malignant Fibrous Histiocytoma Cell Line, COMA Mairal, Aline
2000
121 2 p. 117-123
7 p.
artikel
10 Fluorescence In Situ Hybridization Determination of 22q12–q13 Deletion in Two Intracerebral Ependymomas Rousseau-Merck, Marie-Françoise
2000
121 2 p. 223-227
5 p.
artikel
11 Genetic Characterization of Angiomatoid Fibrous Histiocytoma Identifies Fusion of the FUS and ATF-1 Genes Induced by a Chromosomal Translocation Involving Bands 12q13 and 16p11 Waters, Brenda L
2000
121 2 p. 109-116
8 p.
artikel
12 Inv(12)(q15q24) Scantamburlo, G
2000
121 2 p. 206-207
2 p.
artikel
13 Isochromosome (7)(q10) in Shwachman Syndrome Without MDS/AML and Role of Chromosome 7 Anomalies in Myeloproliferative Disorders Maserati, Emanuela
2000
121 2 p. 167-171
5 p.
artikel
14 Karyotypic Findings in Two Cases of Male Breast Cancer Rudas, Margarethe
2000
121 2 p. 190-193
4 p.
artikel
15 Losses of Heterozygosity in Endometrial Adenocarcinomas Sirchia, Silvia M
2000
121 2 p. 156-162
7 p.
artikel
16 Molecular Cytogenetic Study of a Hemangiopericytoma in a Newborn Dennis, Thomas R
2000
121 2 p. 146-149
4 p.
artikel
17 Mutational Analysis of the NM23.H1 Gene in Human Breast Cancer Cipollini, Giovanna
2000
121 2 p. 181-185
5 p.
artikel
18 New Cytogenetic Data on Bladder Carcinoma Cell Line (CHA89) Revealed by M-FISH Analysis 2000
121 2 p. 228-229
2 p.
artikel
19 p53 Abnormality and Chromosomal Instability in the Same Breast Tumor Cells Sigurdsson, Stefan
2000
121 2 p. 150-155
6 p.
artikel
20 Pentasomy 8 in Pediatric Myelodysplastic Syndrome Wong, Wing-Yen
2000
121 2 p. 220-222
3 p.
artikel
21 Reciprocal Translocation (3;5)(q26;q22) and Possible BCHE Gene Involvement in an Unusual Myelogenous Disorder with both Myeloproliferative and Dysplastic Features Füreder, Wolfgang
2000
121 2 p. 133-138
6 p.
artikel
22 Translocation (5;18) in a Patient with Myelodysplastic Syndrome Sashida, Goro
2000
121 2 p. 230-231
2 p.
artikel
23 Trisomy 4 and Double Minutes in Acute Myeloid Leukemia Govberg, Inna J
2000
121 2 p. 212-215
4 p.
artikel
24 Trisomy 15 Is Frequently Observed as a Minor Clone in Patients with Anemia/ MDS/ NHL and as a Major Clone in Patients with AML Batanian, J.R
2000
121 2 p. 186-189
4 p.
artikel
25 Unusual Breakpoint Distribution of 8p Abnormalities in T-Prolymphocytic Leukemia Sorour, Amani
2000
121 2 p. 128-132
5 p.
artikel
                             25 gevonden resultaten
 
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