| 41 |
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An indolent B-cell lymphoma with t(2;8)(p12;q24) abnormality and absence of C-MYC amplification and TP53 deletion. A new variant?/
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Potti, A
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Elsevier Science Pub. Co. [etc.]
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2003
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| 42 |
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Announcement to contributors/
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Elsevier Science Pub. Co. [etc.]
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2003
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| 43 |
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A Novel Dicentric Deleted Chromosome 21 Arising from Tandem Translocation/
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Robinson, L
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Elsevier Science Pub. Co. [etc.]
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2000
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| 44 |
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A Novel High Mobility Group Protein Gene Is a Candidate for Xp22 Abnormalities in Uterine Leiomyomas and Other Benign Tumors/
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Blank, Cornelia
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Elsevier Science Pub. Co. [etc.]
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2000
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| 45 |
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A novel method for eliminating the melanin pigments from melanoma cells undergoing cytogenetic analysis in cases of uveal melanoma/
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Das, Debashish
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Elsevier Science Pub. Co. [etc.]
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2001
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| 46 |
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A novel t(2;6)(p12;q23) appearing during transformation of follicular lymphoma with t(18;22)(q21;q11) to diffuse large cell lymphoma/
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Yamamoto, K
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Elsevier Science Pub. Co. [etc.]
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2003
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| 47 |
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A novel translocation der(4)t(1;4)(q21;q35) and a marker chromosome in a case of myelodysplastic syndrome/
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Vundinti, B. R
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Elsevier Science Pub. Co. [etc.]
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2003
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| 48 |
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Application of comparative genomic hybridization technique for detection of chromosomal aberrations in benign cystic teratoma/
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Amiel, A
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Elsevier Science Pub. Co. [etc.]
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2003
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| 49 |
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Application of molecular cytogenetic techniques in a case study of human cutaneous metastatic melanoma/
|
Wiltshire, Rodney N
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Elsevier Science Pub. Co. [etc.]
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2001
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| 50 |
|
Application of spectral karyotyping to the analysis of the human chromosome complement of interspecies somatic cell hybrids/
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Matsui, S. i
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Elsevier Science Pub. Co. [etc.]
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2003
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| 51 |
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Are cancers dependent on oncogenes or on aneuploidy?/
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Duesberg, P. H
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Elsevier Science Pub. Co. [etc.]
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2003
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| 52 |
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Are gains of chromosomal regions 7q and 11p important abnormalities in neuroblastoma?/
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Stallings, R. L
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Elsevier Science Pub. Co. [etc.]
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2003
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| 53 |
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A review of the cytogenetics of 58 pediatric brain tumors/
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Roberts, P
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Elsevier Science Pub. Co. [etc.]
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2001
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| 54 |
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Arm-specific multicolor fluorescence in situ hybridization reveals widespread chromosomal instability in glioma cell lines/
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Sallinen, S. L
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Elsevier Science Pub. Co. [etc.]
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2003
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| 55 |
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Array comparative genomic hybridization analysis of myelodysplastic syndromes with complex karyotypes. A technical evaluation/
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Martinez-Ramirez, A
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Elsevier Science Pub. Co. [etc.]
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2003
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| 56 |
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A simple strategy for breakpoint fragment determination in chronic myeloid leukemia/
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Kamel, Azza M
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Elsevier Science Pub. Co. [etc.]
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2001
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| 57 |
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A specific chromosome aberration in a keratoacanthoma/
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Kim, D. K
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Elsevier Science Pub. Co. [etc.]
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2003
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| 58 |
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ATM gene mutations are not involved in medulloblastoma in children/
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Liberzon, E
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Elsevier Science Pub. Co. [etc.]
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2003
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| 59 |
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ATM missense mutations are frequent inpatients with breast cancer/
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Sommer, S. S
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Elsevier Science Pub. Co. [etc.]
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2003
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| 60 |
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A unique AML1 (CBF2A) rearrangement, t(1;21)(p32;q22), observed in a patient with acute myelomonocytic leukemia/
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Cherry, Athena M
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Elsevier Science Pub. Co. [etc.]
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2001
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