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Annals of Human Genetics|October 1, 1986
Genetics of Hunter syndrome: carrier detection, new mutations, segregation and linkage analysisD S Chase, A H Morris, A Ballabio, et al.Annals of Human Genetics|May 1, 1986
Assignment of the gene determining human carbonic anhydrase, CAI, to chromosome 8Y H Edwards, J H Barlow, C P Konialis, et al.Annals of Human Genetics|March 31, 2022
Genetic and environmental correlational structure among metabolic syndrome endophenotypesStacey S Cherny, Frances M K Williams, Gregory LivshitsAnnals of Human Genetics|September 4, 2018
Assessment of candidate folate sensitive-differentially methylated regions in a randomised controlled trial of continued folic acid supplementation during the second and third trimesters of pregnancyAlan Harrison, Kristina Pentieva, Mari Ozaki, et al.Annals of Human Genetics|January 1, 1979
Genetic heterogeneity within an electrophoretic phenotype of phosphoglucose isomerase in a Japanese populationC Satoh, H W MohrenweiserAnnals of Human Genetics|January 1, 1979
Trends in human reproductive wastage in relation to long-term practice of inbreedingP S Rao, S G InbarajAnnals of Human Genetics|October 1, 1975
A genetic analysis of the normal body-height growth and dental development in manN Ryman, J Lindsten, S Leikrans, et al.Annals of Human Genetics|October 1, 1975
The inheritance of scholastic abilities in a sample of twins. II. Genetical analysis of examinations resultsN G MartinAnnals of Human Genetics|June 11, 1999
Linkage disequilibrium at the cystathionine beta synthase (CBS) locus and the association between genetic variation at the CBS locus and plasma levels of homocysteine. The Ears II Group. European Atherosclerosis Research StudyV De Stefano, V Dekou, V Nicaud, et al.Pageof 231