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Developmental Dynamics : an Official Publication of the American Association of Anatomists|May 26, 2022
Fgf8 dosage regulates jaw shape and symmetry through pharyngeal-cardiac tissue relationshipsNathaniel Zbasnik, Katie Dolan, Stephanie A Buczkowski, et al.Evolution & Development|July 12, 2011
Evolution of the Alx homeobox gene family: parallel retention and independent loss of the vertebrate Alx3 geneImelda M McGonnell, Anthony Graham, Joanna Richardson, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2022
A clinical scoring system for early onset (neonatal) Marfan syndromeYuri A Zarate, Shaine A Morris, Anna Blackshare, et al.Proceedings of the National Academy of Sciences of the United States of America|September 18, 2024
Etiology of craniofacial and cardiac malformations in a mouse model of SF3B4-related syndromesShruti Kumar, Eric Bareke, Jimmy Lee, et al.American Journal of Medical Genetics. Part A|August 18, 2017
The role of IQSEC2 in syndromic intellectual disability: Narrowing the diagnostic odysseyBenjamin M Helm, Zoe Powis, Carlos E Prada, et al.Nature Neuroscience|May 4, 2010
OSVZ progenitors of human and ferret neocortex are epithelial-like and expand by integrin signalingSimone A Fietz, Iva Kelava, Johannes Vogt, et al.Pediatric Neurology|May 25, 2020
Epilepsy and Electroencephalographic Abnormalities in SATB2-Associated SyndromeHannah Lewis, Debopam Samanta, Jenny-Li Örsell, et al.Disease Models & Mechanisms|November 9, 2014
Tfap2a-dependent changes in mouse facial morphology result in clefting that can be ameliorated by a reduction in Fgf8 gene dosageRebecca M Green, Weiguo Feng, Tzulip Phang, et al.Seminars in Cell & Developmental Biology|May 22, 2018
The developmental-genetics of canalizationBenedikt Hallgrimsson, Rebecca M Green, David C Katz, et al.Human Mutation|April 14, 2025
Quantitative Phenotype Morbidity Description of SATB2-Associated SyndromeYuri A Zarate, Katherine Bosanko, Amrit Kannan, et al.Pageof 12