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Human Heredity|November 26, 2002
A method for incorporating ages at onset in affected sibpair linkage studiesL Hsu, H Li, J J Houwing-DuistermaatHuman Heredity|November 26, 2002
A novel nonsense mutation of the sedlin gene in a family with spondyloepiphyseal dysplasia tardaYi-Ru Shi, Cheng-Chun Lee, Yu-An Hsu, et al.Human Heredity|July 30, 2002
Statistical properties of Teng and Risch's sibship type tests for detecting an association between disease and a candidate alleleZ Li, M H Gail, D Pee, et al.Human Heredity|July 30, 2002
Models and tests of linkage and association studies of quantitative trait locus for multi-allele marker LociR Fan, J Floros, M XiongHuman Heredity|July 30, 2002
Linkage disequilibrium mapping of quantitative trait loci under truncation selectionM Xiong, R Fan, L JinHuman Heredity|June 12, 1999
Screening for mutations in the promoter and the coding region of the IGFBP1 and IGFBP3 genes in Silver-Russell syndrome patientsK Eggermann, H A Wollmann, J Tomiuk, et al.Human Heredity|July 6, 2000
Prevalence of CCR5 and CCR2 HIV-coreceptor gene polymorphisms in BelgiumF Struyf, I Thoelen, N Charlier, et al.Human Heredity|May 9, 2000
Mapping genes for polygenic disorders: considerations for study design in the complex trait of inflammatory bowel diseaseJ Hampe, T Wienker, P Nürnberg, et al.Human Heredity|May 9, 2000
Model-free analysis and permutation tests for allelic associationsJ H Zhao, D Curtis, P C ShamPageof 237