Showing results (511-520 of 2,368) with videos related to
Sort By:
Pageof 237
Human Heredity|January 1, 1988
Polymorphic restriction sites of type II collagen gene: their location and frequencies in the Finnish populationP Väisänen, K Elima, A Palotie, et al.Human Heredity|August 21, 2014
Using gene genealogies to detect rare variants associated with complex traitsKelly M Burkett, Brad McNeney, Jinko Graham, et al.Human Heredity|November 6, 2015
Estimating the Total Pathogenic Allele Frequency of Autosomal Recessive Disorders in Case of ConsanguinityMarianne A Jonker, Marieke E Teeuw, Wided Kelmemi, et al.Human Heredity|October 6, 2015
A Case Study of Fixed-Effects and Random-Effects Meta-Analysis Models for Genome-Wide Association Studies in Celiac DiseaseRichard S Ahn, Chad GarnerHuman Heredity|May 5, 2012
A unified framework for detecting rare variant quantitative trait associations in pedigree and unrelated individuals via sequence dataDajiang J Liu, Suzanne M LealHuman Heredity|January 1, 1990
Wd(a+) red blood cells in two sisters of a Hei//om Khoisan family in NamibiaP Moores, E Smart, M Marks, et al.Human Heredity|January 1, 1990
Two new orosomucoid (ORM2) variants in JapaneseY Fukuma, S Kashimura, K Umetsu, et al.Human Heredity|January 1, 1990
Presymptomatic exclusion of myotonic dystrophy in a one-generation pedigree of half-siblingsJ Ott, J Caesar, M Mächler, et al.Human Heredity|January 1, 1990
Distribution of human Zn-alpha-2-glycoprotein types in Chinese and Korean populationsM Ding, K Umetsu, N Nakayashiki, et al.Human Heredity|January 1, 1977
An analysis of red cell enzymatic markers in the province of Bologna (Italy)M Beretta, C Barberio, G Ranzani, et al.Pageof 237