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Human Heredity|May 1, 1994
Low frequency of the delta F508 mutation in Finno-Ugrian and Baltic populationsC Wennberg, V KucinskasHuman Heredity|January 1, 1976
Genetic studies among the endogamous groups of Lohanas of North and West IndiaH M Bhatia, S R Shanbagh, A J Baxi, et al.Human Heredity|October 26, 2005
A novel autosomal recessive non-syndromic deafness locus, DFNB66, maps to chromosome 6p21.2-22.3 in a large Tunisian consanguineous familyAbdelaziz Tlili, Minna Männikkö, Ilhem Charfedine, et al.Human Heredity|January 14, 2010
A Likelihood-Based Approach for Missing Genotype DataGina M D'Angelo, M Ilyas Kamboh, Eleanor FeingoldHuman Heredity|July 6, 2000
Gene-environment interaction and the mapping of complex traits: some statistical models and their implicationsS W GuoHuman Heredity|July 6, 2000
Estimation of transmission probabilities in families ascertained through a proband with variable age-at-onset disease: application to the HLA A, B and DR loci in Finnish families with type 1 diabetes. The DiMe Study GroupJ Pitkäniemi, P Onkamo, E Arjas, et al.Human Heredity|July 6, 2000
Monilethrix: mutational hotspot in the helix termination motif of the human hair basic keratin 6L Horev, B Glaser, A Metzker, et al.Human Heredity|May 9, 2000
Fine mapping of the human biotinidase gene and haplotype analysis of five common mutationsS H Blanton, A Pandya, B L Landa, et al.Human Heredity|May 9, 2000
alpha-thalassemia in Bantu population from Congo-Brazzaville: its interaction with sickle cell anemiaR Mouélé, O Pambou, J Feingold, et al.Human Heredity|May 9, 2000
Effects of misspecification of allele frequencies on the type I error rate of model-free linkage analysisD M Mandal, A F Wilson, R C Elston, et al.Pageof 237