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Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 3, 2001
Down syndrome congenital heart disease: a narrowed region and a candidate geneG M Barlow, X N Chen, Z Y Shi, et al.American Journal of Medical Genetics. Part A|October 12, 2013
Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS-FREM complex disordersDenny Schanze, Magdalena Harakalova, Cathy A Stevens, et al.Plos One|October 11, 2012
Results of genome-wide analyses on neurodevelopmental phenotypes at four-year follow-up following cardiac surgery in infancyDaniel S Kim, Ian B Stanaway, Ramakrishnan Rajagopalan, et al.Journal of the National Cancer Institute|May 8, 2003
Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndromeLisa L Wang, Anu Gannavarapu, Claudia A Kozinetz, et al.Brain : a Journal of Neurology|April 20, 2021
Disruption of the blood-brain barrier in 22q11.2 deletion syndromeAlexis M Crockett, Sean K Ryan, Adriana Hernandez Vásquez, et al.Psychiatry Research. Neuroimaging|September 3, 2017
White matter microstructural deficits in 22q11.2 deletion syndromeDavid R Roalf, J Eric Schmitt, Simon N Vandekar, et al.The Journal of Pediatrics|December 17, 2017
Hearing Loss after Cardiac Surgery in Infancy: An Unintended Consequence of Life-Saving CareMadison A Grasty, Richard F Ittenbach, Carol Knightly, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 28, 2020
Early language measures associated with later psychosis features in 22q11.2 deletion syndromeCynthia B Solot, Tyler M Moore, Terrence Blaine Crowley, et al.Archives of Pediatrics & Adolescent Medicine|January 6, 2010
Novel influenza A(H1N1) in a pediatric health care facility in New York City during the first wave of the 2009 pandemicYolanda Miroballi, J Scott Baird, Sheemon Zackai, et al.AJNR. American Journal of Neuroradiology|June 21, 2014
Incidental radiologic findings in the 22q11.2 deletion syndromeJ E Schmitt, J J Yi, D R Roalf, et al.Pageof 63