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Cytogenetics and Cell Genetics|January 1, 1996
FISH localization of the soluble thymidine kinase gene (TK1) to human 17q25, a region of chromosomal loss in sporadic breast tumorsE M Petty, D E Miller, A L Grant, et al.Genomics|June 1, 1992
Refined localization of human connexin32 gene locus, GJB1, to Xq13.1I A Corcos, R G Lafrenière, C R Begy, et al.Nature|October 31, 1991
A de novo Alu insertion results in neurofibromatosis type 1M R Wallace, L B Andersen, A M Saulino, et al.Clinical Genetics|February 1, 1986
Population cytogenetics of autosomal fragile sitesP Petit, J P Fryns, H van den Berghe, et al.Cancer Genetics and Cytogenetics|March 15, 1986
The Philadelphia chromosome: a model of cancer and molecular cytogeneticsA A Sandberg, R M Gemmill, B K Hecht, et al.Genes, Chromosomes & Cancer|February 15, 2001
Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinomaJ M Fang, M F Arlt, A C Burgess, et al.Genomics|December 15, 1996
Tissue distribution, genomic structure, and chromosome mapping of mouse and human eukaryotic initiation factor 4E-binding proteins 1 and 2K Tsukiyama-Kohara, S M Vidal, A C Gingras, et al.Blood|December 1, 1985
Leukemia with Down's syndrome: translocation between chromosomes 1 and 19 in acute myelomonocytic leukemia following transient congenital myeloproliferative syndromeR Morgan, F Hecht, M L Cleary, et al.Birth Defects Original Article Series|January 1, 1976
Human centromere mapping using teratoma dataJ Ott, F Hecht, D Linder, et al.Blood|March 1, 1986
Cytogenetic and immunophenotypic analysis of cell lines established from patients with T cell leukemia/lymphomaS D Smith, R Morgan, M P Link, et al.Pageof 22