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Annals of Human Genetics|January 21, 2015
Effectiveness of shrinkage and variable selection methods for the prediction of complex human traits using data from distantly related individualsSwetlana Berger, Paulino Pérez-Rodríguez, Yogasudha Veturi, et al.Annals of Human Genetics|October 24, 2017
Influence of Apolipoprotein E polymorphism on susceptibility of Wilson diseaseShubhrajit Roy, Kausik Ganguly, Prosenjit Pal, et al.Annals of Human Genetics|September 29, 2015
Y-Chromosomal Lineages of Latvians in the Context of the Genetic Variation of the Eastern-Baltic RegionLiana Pliss, Līga Timša, Siiri Rootsi, et al.Annals of Human Genetics|October 1, 2015
In Silico Prediction of the Effects of Mutations in the Human Mevalonate Kinase Gene: Towards a Predictive Framework for Mevalonate Kinase DeficiencyClaire Browne, David J TimsonAnnals of Human Genetics|October 1, 2015
Twenty-One Novel EGFR Kinase Domain variants in Patients with Nonsmall Cell Lung CancerMarcia A Hasenahuer, Gustavo Parisi, Marien Gautier, et al.Annals of Human Genetics|July 25, 2017
Disease-Causing Variants in the ATL1 Gene Are a Rare Cause of Hereditary Spastic Paraplegia among Czech PatientsAnna Uhrová Mészárosová, Dagmar Grečmalová, Michaela Brázdilová, et al.Annals of Human Genetics|August 9, 2017
Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, ChinaJianfen Luo, Xiaohui Bai, Fengguo Zhang, et al.Annals of Human Genetics|November 17, 2015
The Quantitative-MFG Test: A Linear Mixed Effect Model to Detect Maternal-Offspring Gene InteractionsMichelle M Clark, John Blangero, Thomas D Dyer, et al.Annals of Human Genetics|November 18, 2017
Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophreniaMariam M Al Eissa, Alessia Fiorentino, Sally I Sharp, et al.Pageof 231