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Human Genetics|January 1, 1990
Cloning and sequence analysis of the human parathyroid hormone gene regionA Reis, W Hecht, R Gröger, et al.Biology of Reproduction|April 18, 1998
Molecular cloning and characterization of P47, a novel boar sperm-associated zona pellucida-binding protein homologous to a family of mammalian secretory proteinsM Ensslin, T Vogel, J J Calvete, et al.Human Mutation|March 25, 1999
Mutation analysis in 46 German families with familial hypercholesterolemia: identification of 8 new mutations. Mutations in brief no. 226. OnlineM Ebhardt, H Schmidt, T Doerk, et al.Klinische Wochenschrift|July 15, 1987
Autopsy findings in AIDS--a histopathological analysis of fifty casesS Falk, H L Schmidts, H Müller, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|April 1, 1989
[DNA diagnosis of monogene hereditary diseases exemplified by phenylketonuria and mucoviscidosis]F K Trefz, U Lichter-Konecki, M Krawczak, et al.Human Genetics|January 1, 1985
Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IXB Zoll, J Arnemann, M Krawczak, et al.Biology of Reproduction|May 30, 2003
Generation and characterization of a transgenic mouse with a functional human TSPYS Schubert, B Skawran, F Dechend, et al.Human Mutation|July 20, 2001
Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndromeJ M Hertz, I Juncker, U Persson, et al.American Journal of Human Genetics|December 1, 1987
Segregation of all four major fibrillar collagen genes in the Marfan syndromeD J Ogilvie, B P Wordsworth, L M Priestley, et al.Emerging Infectious Diseases|July 31, 2012
Population diversity among Bordetella pertussis isolates, United States, 1935-2009Amber J Schmidtke, Kathryn O Boney, Stacey W Martin, et al.Pageof 25