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The American Journal of Medicine|June 1, 1984
Chromosome analysis in hematologic disorders. The leukemiasA A Sandberg, R Morgan, C Berger, et al.Clinical Genetics|March 1, 1986
Genetic control over fragile X chromosome expressionF Hecht, J P Fryns, R F Vlietinck, et al.Annals of Human Genetics|November 1, 1976
Estimating distances from the centromere by means of benign ovarian teratomas in manJ Ott, D Linder, B K McCaw, et al.Journal of Developmental and Behavioral Pediatrics : JDBP|January 1, 2013
Early identification of young children with hearing loss in federally qualified health centersParul Bhatia, Sandra Mintz, Barbara F Hecht, et al.Tissue Antigens|January 1, 1987
The human sex ratio: increase in first-born males to parents with shared HLA-DR antigensR M Radvany, N Vaisrub, C Ober, et al.Cancer Genetics and Cytogenetics|January 1, 1985
The Philadelphia (Ph) chromosome in leukemia. I. A new mechanism due to interstitial deletion and insertion in chronic myelocytic leukemiaF Hecht, R Morgan, S L Schrier, et al.Neurofibromatosis|January 1, 1988
Hereditary intestinal neurofibromatosis. I. A distinctive genetic diseaseR Heimann, A Verhest, J Verschraegen, et al.Cancer Genetics and Cytogenetics|September 1, 1982
Translocations involving chromosomes #3 and #12: hematologic diseases associated with abnormalities of these chromosomesA A Sandberg, B K Hecht, S M Ondreyco, et al.American Journal of Medical Genetics|November 1, 1993
Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literatureH A Hales, C M Peterson, J Carey, et al.Cancer Genetics and Cytogenetics|June 1, 1988
Inversion of chromosome 5 long arm in region of cell growth gene cluster in hematologic disordersR Morgan, T A Walter, H J Decker, et al.Pageof 16