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Human Genetics|March 1, 1987
Alpha-thalassemia haplotypes in the Algerian populationT Henni, F Morlé, B Lopez, et al.Human Genetics|October 3, 2018
Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorderN H Chapman, R A Bernier, S J Webb, et al.Human Genetics|September 7, 2018
Genetic landscape of isolated pediatric cataracts: extreme heterogeneity and variable inheritance patterns within genesLinda M Reis, Elena V SeminaHuman Genetics|May 23, 2019
Therapeutic application of the CRISPR system: current issues and new prospectsMinyoung Lee, Hyongbum KimHuman Genetics|May 10, 2019
De novo emergence and potential function of human-specific tandem repeats in brain-related lociKwondo Kim, Sohyun Bang, DongAhn Yoo, et al.Human Genetics|May 11, 2019
A commonly occurring genetic variant within the NPLOC4-TSPAN10-PDE6G gene cluster is associated with the risk of strabismusDenis Plotnikov, Rupal L Shah, Jamille N Rodrigues, et al.Human Genetics|May 11, 2019
An update on the genetics of ocular colobomaAisha S ALSomiry, Cheryl Y Gregory-Evans, Kevin Gregory-EvansHuman Genetics|March 1, 1988
Linkage disequilibrium analyses and restriction mapping of four RFLPs at the pro alpha 2(I) collagen locus: lack of correlation between linkage disequilibrium and physical distanceA L Børresen, P Møller, K BergHuman Genetics|February 15, 2019
Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmiaJ Plaisancié, F Ceroni, R Holt, et al.Human Genetics|October 1, 1988
Sorting of chromosomes by magnetic separationG Dudin, E W Steegmayer, P Vogt, et al.Pageof 957