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Molecular Syndromology|May 20, 2016
X-Linked Candidate Genes for a Ciliopathy-Like DisorderAshleigh R Pavey, Thierry Vilboux, Holly E Babcock, et al.Plos One|July 9, 2014
aldh7a1 regulates eye and limb development in zebrafishHolly E Babcock, Sunit Dutta, Ramakrishna P Alur, et al.American Journal of Medical Genetics. Part A|April 22, 2025
New Phenotypic Features in FGFR1-Related Osteoglophonic DysplasiaAmna A Othman, Holly E Babcock, Corey S Gill, 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.The Journal of Clinical Investigation|January 26, 2021
Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humansThuy-Linh Le, Louise Galmiche, Jonathan Levy, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 10, 2020
De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathyChiara Klöckner, Heinrich Sticht, Pia Zacher, et al.Pageof 1