Showing results (471-480 of 627) with videos related to
Sort By:
Pageof 63
American Journal of Medical Genetics. Part A|July 29, 2018
Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patientsMark D Levin, Sulagna C Saitta, Karen W Gripp, et al.The Annals of Thoracic Surgery|May 10, 2014
Patient genotypes impact survival after surgery for isolated congenital heart diseaseDaniel Seung Kim, Jerry H Kim, Amber A Burt, et al.American Journal of Human Genetics|August 3, 2010
A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21)Molly B Sheridan, Takema Kato, Chad Haldeman-Englert, et al.The Journal of Thoracic and Cardiovascular Surgery|December 26, 2015
Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survivalDaniel Seung Kim, Jerry H Kim, Amber A Burt, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 27, 2020
De novo loss-of-function variants in X-linked MED12 are associated with Hardikar syndrome in femalesDong Li, Alanna Strong, Kaitlyn M Shen, et al.Autism Research : Official Journal of the International Society for Autism Research|June 23, 2020
Mapping the Relationship between Dysmorphology and Cognitive, Behavioral, and Developmental Outcomes in Children with Autism Spectrum DisorderLin H Tian, Lisa D Wiggins, Laura A Schieve, et al.American Journal of Medical Genetics. Part A|August 29, 2018
Variable Clinical Manifestations of Xia-Gibbs syndrome: Findings of Consecutively Identified Cases at a Single Children's HospitalAlyssa L Ritter, Carey McDougall, Cara Skraban, et al.Scientific Reports|July 24, 2020
Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR)Steven Pastor, Oanh Tran, Andrea Jin, et al.American Journal of Medical Genetics. Part A|May 7, 2011
Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25Deepika D'Cunha Burkardt, Jill A Rosenfeld, Maria L Helgeson, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2024
Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participantsAmir Hossein Saeidian, Michael E March, Leila Youssefian, et al.Pageof 63