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Annals of Human Genetics|July 26, 2017
The Impact of FOXP3 Polymorphism on the Risk of Allergic Rhinitis: A Meta-AnalysisGuimin Zhang, Di Zhang, Wenjie Shi, et al.Annals of Human Genetics|January 1, 1989
Efficient computation of lod scores: genotype elimination, genotype redefinition, and hybrid maximum likelihood algorithmsK Lange, D E WeeksAnnals of Human Genetics|September 13, 2017
Construction of an Exome-Wide Risk Score for Schizophrenia Based on a Weighted Burden TestDavid CurtisAnnals of Human Genetics|September 1, 2017
Interaction Between Val158Met Catechol-O-Methyltransferase Polymorphism and Social Cognitive Functioning in Schizophrenia: Pilot StudyAneta Tylec, Witold Jeleniewicz, Ann Mortimer, et al.Annals of Human Genetics|December 3, 2015
Incorporating Hardy-Weinberg Equilibrium Law to Enhance the Association Strength for Ordinal Trait Genetic StudyWei Zhang, Qizhai LiAnnals of Human Genetics|May 1, 1989
An investigation of the properties and possible clinical significance of the lysosomal alpha-glucosidase GAA*2 alleleD M Swallow, M Kroos, A T Van der Ploeg, et al.Annals of Human Genetics|May 1, 1989
An investigation of the possible influence of neutral alpha-glucosidases on the clinical heterogeneity of glycogenosis type IIA T Van der Ploeg, M A Kroos, D M Swallow, et al.Annals of Human Genetics|May 1, 1989
Chromosome maps of man and mouse. IVA G Searle, J Peters, M F Lyon, et al.Annals of Human Genetics|October 24, 2017
How many cases of disease in a pedigree imply familial disease?Frank Dudbridge, Suzanne J Brown, Lynley Ward, et al.Annals of Human Genetics|September 4, 2018
Update of spectrum c.35delG and c.-23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing lossFatemeh Azadegan-Dehkordi, Reza Ahmadi, Mahbobeh Koohiyan, et al.Pageof 231