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Annals of Human Genetics|October 1, 1987
Breakpoint distribution in constitutional chromosome rearrangements with respect to fragile sitesB Porfirio, B Dallapiccola, L TerrenatoAnnals of Human Genetics|May 1, 1986
The C8A and C8B loci are closely linked on chromosome 1S Rogde, B Olaisen, T Gedde-Dahl, et al.Annals of Human Genetics|May 8, 2021
Mutation spectrum of hereditary myopathies in Turkish patients and novel variantsHanife Saat, Ibrahim SahinAnnals of Human Genetics|May 20, 2021
An analysis of the demographic history of the risk allele R4810K in RNF213 of moyamoya diseaseKae Koganebuchi, Kimitoshi Sato, Kiyotaka Fujii, et al.Annals of Human Genetics|May 23, 2015
Trans-ethnic meta-analysis identifies common and rare variants associated with hepatocyte growth factor levels in the Multi-Ethnic Study of Atherosclerosis (MESA)Nicholas B Larson, Cecilia Berardi, Paul A Decker, et al.Annals of Human Genetics|June 24, 2015
Identification of Two Homozygous Sequence Variants in the COL7A1 Gene Underlying Dystrophic Epidermolysis Bullosa by Whole-Exome Analysis in a Consanguineous FamilyRehab Serafi, Musharraf Jelani, Mona M Almramhi, et al.Annals of Human Genetics|September 15, 2021
The hazards of genotype imputation in chromosomal regions under selection: A case study using the Lactase gene regionAminah T Ali, Anke Liebert, Winston Lau, et al.Annals of Human Genetics|May 14, 2020
MEFV c.2230G>T p.(Ala744Ser) rs61732874 previously misclassified as pathogenic variant due to lack of a population specific databaseLamia Alsubaie, Randa Alkhalaf, Taghrid Aloraini, et al.Annals of Human Genetics|May 13, 2020
Identification and functional characterization of CYP4V2 genetic variants exhibiting decreased activity of lauric acid metabolismYazun Bashir Jarrar, Jae-Gook Shin, Su-Jun LeeAnnals of Human Genetics|February 22, 2005
Generating genetic risk scores from intermediate phenotypes for use in association studies of clinically significant endpointsB D Horne, J L Anderson, J F Carlquist, et al.Pageof 231