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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.The New England Journal of Medicine|September 9, 1990
Absence of need for amniocentesis in patients with elevated levels of maternal serum alpha-fetoprotein and normal ultrasonographic examinationsA S Nadel, J K Green, L B Holmes, et al.Teratology|March 15, 2000
Digit effects produced by prenatal exposure to antiepileptic drugsM C Lu, M D Sammel, R H Cleveland, et al.The Journal of Pediatrics|April 1, 1987
Predictive value of minor anomalies. I. Association with major malformationsK A Leppig, M M Werler, C I Cann, 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.Pageof 26