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Journal of Developmental Biology|July 21, 2021
A Novel Mutation in Cse1l Disrupts Brain and Eye Development with Specific Effects on Pax6 ExpressionLauren E Blizzard, Chelsea Menke, Shaili D Patel, et al.
American Journal of Medical Genetics. Part A|September 15, 2021
Genetic and phenotypic heterogeneity in KIAA0753-related ciliopathiesKatherine A Inskeep, Yuri A Zarate, Danielle Monteil, et al.
Plos One|June 9, 2025
Genetic analysis and functional assessment of a TGFBR2 variant in micrognathia and cleft palateJes-Rite Michaels, Paul P R Iyyanar, Ammar Husami, et al.
Genetica|December 29, 2004
Genetic mapping and ENU mutagenesisDavid R Beier, Bruce J Herron
Genome Biology|February 28, 2002
2001: a mouse genome odysseyDavid R Beier, Bruce J Herron
Genome Research|May 5, 2012
Mutation mapping and identification by whole-genome sequencingIgnaty Leshchiner, Kristen Alexa, Peter Kelsey, et al.
HGG Advances|September 19, 2025
Bi-allelic INTU variants define a ciliopathy disorder characterized by orofacial, digital, and cardiac anomaliesRebekah Rushforth, Kurt Reynolds, Steven I Estes, et al.
American Journal of Medical Genetics. Part A|March 17, 2025
The Society for Craniofacial Genetics and Developmental Biology 47th Annual MeetingPaul A Trainor, Timothy C Cox, David E Clouthier, et al.
Plos One|March 15, 2017
Unique spatiotemporal requirements for intraflagellar transport genes during forebrain developmentJohn Snedeker, Elizabeth N Schock, Jamie N Struve, et al.
Development (Cambridge, England)|January 11, 2018
A mutation in <i>Ccdc39</i> causes neonatal hydrocephalus with abnormal motile cilia development in miceZakia Abdelhamed, Shawn M Vuong, Lauren Hill, et al.
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