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American Journal of Medical Genetics. Part A|October 18, 2011
A therapeutic trial of pro-methylation dietary supplements in Angelman syndromeLynne M Bird, Wen-Hann Tan, Carlos A Bacino, et al.BMJ Open|December 31, 2017
Identifying and understanding the health and social care needs of older adults with multiple chronic conditions and their caregivers: a protocol for a scoping reviewElana Commisso, Katherine S McGilton, Ana Patricia Ayala, et al.Human Molecular Genetics|May 12, 2011
Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3Xiaoming Wang, Portia A McCoy, Ramona M Rodriguiz, et al.Molecular Cytogenetics|April 7, 2012
Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disordersPatrícia Bs Celestino-Soper, Cindy Skinner, Richard Schroer, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2006
Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridizationTrilochan Sahoo, Sau Wai Cheung, Patricia Ward, et al.European Journal of Human Genetics : EJHG|May 23, 2013
Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testingJoanna Wiszniewska, Weimin Bi, Chad Shaw, et al.Journal of Medicinal Chemistry|May 3, 2002
Identification of a nonsteroidal liver X receptor agonist through parallel array synthesis of tertiary aminesJon L Collins, Adam M Fivush, Michael A Watson, et al.American Journal of Medical Genetics. Part A|July 4, 2007
Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogeneticsSau W Cheung, Chad A Shaw, Daryl A Scott, et al.Journal of Anatomy|November 7, 2023
What do brain endocasts tell us? A comparative analysis of the accuracy of sulcal identification by experts and perspectives in palaeoanthropologyNicole Labra, Aurélien Mounier, Yann Leprince, et al.Human Molecular Genetics|August 26, 2011
Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHEPatricia B S Celestino-Soper, Chad A Shaw, Stephan J Sanders, et al.Pageof 105