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American Journal of Medical Genetics. Part A|June 20, 2012
Middle and inner ear malformations in mutation-proven branchio-oculo-facial (BOF) syndrome: case series and review of the literatureMelissa T Carter, Susan Blaser, Blake Papsin, et al.Journal of Autism and Developmental Disorders|July 12, 2012
Parents' perspectives on participating in genetic research in autismMagan Trottier, Wendy Roberts, Irene Drmic, et al.Birth Defects Research. Part B, Developmental and Reproductive Toxicology|December 14, 2011
Incidence and nature of testicular toxicity findings in pharmaceutical developmentJennifer C Sasaki, Robert E Chapin, David Gregory Hall, et al.Radiographics : a Review Publication of the Radiological Society of North America, Inc|January 20, 2004
Detection of fetal structural abnormalities with US during early pregnancyKatherine W Fong, Ants Toi, Shia Salem, et al.Prenatal Diagnosis|June 6, 2024
Associations and outcomes of prenatally detected rhombencephalosynapsisYada Kunpalin, Elka Miller, Kamini Raghuram, et al.Pediatric Blood & Cancer|September 13, 2018
"A change in perspective": Exploring the experiences of adolescents with hereditary tumor predispositionEvan Weber, Cheryl Shuman, Jonathan D Wasserman, et al.Developmental Biology|June 14, 2008
Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentaeLin Guo, Sanaa Choufani, Jose Ferreira, et al.American Journal of Medical Genetics. Part A|September 12, 2012
Interstitial deletion of 11q-implicating the KIRREL3 gene in the neurocognitive delay associated with Jacobsen syndromeAndrea Guerin, Dimitri J Stavropoulos, Yaser Diab, et al.Eye (London, England)|September 17, 2021
Gene therapy: perspectives from young adults with Leber's congenital amaurosisMelanie P Napier, Kavin Selvan, Robin Z Hayeems, et al.Mitochondrion|October 6, 2010
Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganizationJessie M Cameron, Valeriy Levandovskiy, Nevena Mackay, et al.Pageof 45