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Annals of Human Genetics|July 1, 1976
The genetics of specific reading disabilityJ M Finucci, J T Guthrie, A L Childs, et al.Annals of Human Genetics|July 1, 1976
A matrix method for calculating recurrence risks of unilocal disorders for genetic counsellingD R Bolling, G A Chase, E A MurphyAnnals of Human Genetics|July 1, 1976
Chromatid exchanges in ataxia telangiectasia, Bloom syndrome, Werner syndrome, and xeroderma pigmentosumC R Bartram, T Koske-Westphal, E PassargeAnnals of Human Genetics|April 17, 1998
Molecular characterization of isochromosomes of XqR S James, P Dalton, K Gustashaw, et al.Annals of Human Genetics|April 17, 1998
Development of a microsatellite-based approach to co-segregation analysis of familial hypercholesterolaemic kindredsL Haddad, L B Day, J Attwood, et al.Annals of Human Genetics|May 23, 2015
Genetic association and altered gene expression of osteoprotegerin in otosclerosis patientsSaurabh Priyadarshi, Chinmay Sundar Ray, Narayan Chandra Biswal, et al.Annals of Human Genetics|July 1, 1997
Genetic contribution of the HLA region to the familial clustering of coeliac diseaseF Petronzelli, M Bonamico, P Ferrante, et al.Annals of Human Genetics|July 1, 1997
Alpha coat protein COPA (HEP-COP): presence of an Alu repeat in cDNA and identity of the amino terminus to xeninV T Chow, H H QuekAnnals of Human Genetics|May 12, 2015
SVSI: fast and powerful set-valued system identification approach to identifying rare variants in sequencing studies for ordered categorical traitsWenjian Bi, Guolian Kang, Yanlong Zhao, et al.Pageof 231