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American Journal of Medical Genetics. Part A|January 19, 2008
Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearanceMałgorzata J M Nowaczyk, Melissa T Carter, Jie Xu, et al.Science (New York, N.Y.)|August 10, 2002
Recent segmental duplications in the human genomeJeffrey A Bailey, Zhiping Gu, Royden A Clark, et al.Trials|March 26, 2021
Hematologists' barriers and enablers to screening and recruiting patients to a chimeric antigen receptor (CAR) T cell therapy trial: a theory-informed interview studyGisell Castillo, Manoj Lalu, Sarah Asad, et al.American Journal of Medical Genetics. Part A|May 3, 2023
Uniparental disomy of multiple chromosomes in two cases with a complex phenotypeKatarzyna Polonis, Jaime L Lopes, Huong Cabral, et al.American Journal of Medical Genetics. Part A|April 24, 2013
Clinical comparison of overlapping deletions of 19p13.3Hiba Risheg, Romela Pasion, Stephanie Sacharow, et al.Genome Research|June 21, 2005
Punctuated duplication seeding events during the evolution of human chromosome 2p11Julie E Horvath, Cassandra L Gulden, Rhea U Vallente, et al.American Journal of Human Genetics|July 11, 2006
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genomeDevin P Locke, Andrew J Sharp, Steven A McCarroll, et al.Journal of Agricultural and Food Chemistry|September 17, 2025
Phenylglyoxal-induced Ana o 3 Modification Reduces Antibody Binding with Minimal Alteration in Protein StructureC Nacaya Brown, Tien Thuy Vuong, Austin T Weigle, et al.BMJ Open|March 20, 2021
Navigating choice in the face of uncertainty: using a theory informed qualitative approach to identifying potential patient barriers and enablers to participating in an early phase chimeric antigen receptor T (CAR-T) cell therapy trialGisell Castillo, Manoj M Lalu, Sarah Asad, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2018
Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)Darrel Waggoner, Karen E Wain, Adrian M Dubuc, et al.Pageof 10