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Blood Cells, Molecules & Diseases|August 3, 2001
Rapid identification of hemoglobin variants by electrospray ionization mass spectrometryB J Wild, B N Green, E K Cooper, et al.
Human Reproduction (Oxford, England)|October 1, 1992
Preimplantation diagnosis of a human beta-globin transgene in biopsied trophectoderm cells and blastomeres of the mouse embryoS A Sheardown, I Findlay, A Turner, et al.
American Journal of Human Genetics|January 23, 1999
Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mappingM Ohadi, M R Lalloz, P Sham, et al.
Journal of Hepatology|February 12, 1998
Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosisC Datz, M R Lalloz, W Vogel, et al.
Human Genetics|April 4, 2000
Molecular analysis of the genotype-phenotype relationship in factor X deficiencyD S Millar, L Elliston, P Deex, et al.
Advances in Experimental Medicine and Biology|December 19, 2007
Mutation of the von Hippel-Lindau gene alters human cardiopulmonary physiologyT G Smith, J T Brooks, G M Balanos, et al.
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