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American Journal of Medical Genetics. Part A|October 14, 2003
GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome regionColleen A Morris, Carolyn B Mervis, Holly H Hobart, et al.JCI Insight|January 23, 2024
Syntaxin1A overexpression and pain insensitivity in individuals with 7q11.23 duplication syndromeMichael J Iadarola, Matthew R Sapio, Amelia J Loydpierson, et al.Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Identifying individuals at risk for surgical supravalvar aortic stenosis by polygenic risk score with graded phenotypingD Liu, C B Mervis, M D Levin, et al.Cell|July 12, 1996
LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognitionJ M Frangiskakis, A K Ewart, C A Morris, et al.American Journal of Human Genetics|June 21, 2008
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11Christian R Marshall, Edwin J Young, Ariel M Pani, et al.Journal of the American Heart Association|January 31, 2024
Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren SyndromeDelong Liu, Charles J Billington, Neelam Raja, et al.Pageof 13