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Annals of Human Genetics|February 8, 2019
Identification of a novel mutation in EXT2 in a fourth-generation Korean family with multiple osteochondromas and overview of mutation spectrumAram Yang, Jinsup Kim, Ja-Hyun Jang, et al.Annals of Human Genetics|October 7, 2020
A role for the MEGF6 gene in predisposition to osteoporosisCraig C Teerlink, Michael J Jurynec, Rolando Hernandez, et al.Annals of Human Genetics|May 1, 1986
Males, females and hermaphrodites. An inaugural lecture delivered by Professor Ursula Mittwoch at University College London on 24 October 1985U MittwochAnnals of Human Genetics|February 13, 2018
A novel homozygous missense variant in NECTIN4 (PVRL4) causing ectodermal dysplasia cutaneous syndactyly syndromeFarooq Ahmad, Abdul Nasir, Holger Thiele, et al.Annals of Human Genetics|January 1, 1985
Mapping of the gene coding for the human GM2 activator protein to chromosome 5J Burg, E Conzelmann, K Sandhoff, et al.Annals of Human Genetics|January 1, 1985
Genetic and population structure of four Sardinian villagesA Piazza, W R Mayr, L Contu, et al.Annals of Human Genetics|December 22, 2015
Exploring the Major Sources and Extent of Heterogeneity in a Genome-Wide Association Meta-AnalysisYu-Fang Pei, Qing Tian, Lei Zhang, et al.Annals of Human Genetics|September 26, 2015
Ethnicity-Based Differences in the Association of LOXL1 Polymorphisms with Pseudoexfoliation/Pseudoexfoliative Glaucoma: A Meta-AnalysisPanayiota Founti, Anna-Bettina Haidich, Anthoula Chatzikyriakidou, et al.Annals of Human Genetics|September 26, 2015
Hypovitaminosis D in a Young Lebanese Population: Effect of GC Gene Polymorphisms on Vitamin D and Vitamin D Binding Protein LevelsMyrna Medlej-Hashim, Rania Jounblat, Aline Hamade, et al.Annals of Human Genetics|October 1, 2015
Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of HomozygosityNizar Ben Halim, Majdi Nagara, Béatrice Regnault, et al.Pageof 231