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Human Mutation|June 10, 2016
The SSV Evaluation System: A Tool to Prioritize Short Structural Variants for Studies of Possible Regulatory and Causal VariantsRobert Saul, Michael W Lutz, Daniel K Burns, et al.American Journal of Medical Genetics. Part A|November 21, 2013
Genetic services and attitudes in primary care pediatricsMichael L Rinke, Natalie Mikat-Stevens, Robert Saul, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|June 17, 2015
A cytosine-thymine (CT)-rich haplotype in intron 4 of SNCA confers risk for Lewy body pathology in Alzheimer's disease and affects SNCA expressionMichael W Lutz, Robert Saul, Colton Linnertz, et al.Human Molecular Genetics|September 13, 2013
A mutation in a ganglioside biosynthetic enzyme, ST3GAL5, results in salt & pepper syndrome, a neurocutaneous disorder with altered glycolipid and glycoprotein glycosylationLuigi Boccuto, Kazuhiro Aoki, Heather Flanagan-Steet, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|September 28, 2014
African-American TOMM40'523-APOE haplotypes are admixture of West African and Caucasian allelesAllen D Roses, Michael W Lutz, Ann M Saunders, et al.Pageof 1