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Clinical Genetics|February 1, 1978
Prenatal diagnosis of 5p-K David, S Kaffe, L Strauss, et al.
International Archives of Allergy and Applied Immunology|January 1, 1975
Intracellular localization of the migration inhibitory factor (MIF) in a long-term human lymphoid cell lineM B Prystowsky, C F Sorokin, W S Ceglowski, et al.
The New England Journal of Medicine|October 23, 1975
Cytogenetics of fetal wastageH J Kim, L Y Hsu, S Paciuc, et al.
American Journal of Human Genetics|November 1, 1975
Kniest syndrome with dominant inheritance and mucopolysacchariduriaH J Kim, N G Beratis, P Brill, et al.
American Journal of Medical Genetics|May 2, 1997
Paternal uniparental disomy for chromosome 14: a case report and reviewP D Cotter, S Kaffe, L D McCurdy, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 2, 2000
Cloning and characterization of human PREB; a gene that maps to a genomic region associated with trisomy 2p syndromeC L Taylor Clelland, B Levy, J M McKie, et al.
Science (New York, N.Y.)|December 19, 1975
Vitamin B6-responsive and -unresponsive cystathioninuria: two variant molecular formsT A Pascal, G E Gaull, N G Beratis, et al.
Cancer Research|August 1, 1978
Observations on cell lines derived from a patient with Hodgkin's diseaseC Friend, W Marovitz, G Henie, et al.
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