Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Daryl A Scott

Showing results (21-30 of 128) with videos related to

Pageof 13
Sort By:
American Journal of Medical Genetics. Part A|July 7, 2022
Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic herniaYoel Gofin, Xiaonan Zhao, Amanda Gerard, et al.
American Journal of Medical Genetics. Part A|July 17, 2009
A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorderJaime M Williams, Tyler F Beck, David M Pearson, et al.
Development (Cambridge, England)|June 28, 2015
Stromal Fat4 acts non-autonomously with Dchs1/2 to restrict the nephron progenitor poolMazdak Bagherie-Lachidan, Antoine Reginensi, Qun Pan, et al.
Human Molecular Genetics|March 27, 2021
RERE deficiency contributes to the development of orofacial clefts in humans and miceBum Jun Kim, Hitisha P Zaveri, Peter N Kundert, et al.
Plos One|April 18, 2017
Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disabilityChristina Grau, Molly Starkovich, Mahshid S Azamian, et al.
European Journal of Human Genetics : EJHG|September 5, 2025
Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+)E Andres Rivera-Munoz, Xiaonan E Zhao, Jill A Rosenfeld, et al.
American Journal of Medical Genetics. Part A|July 8, 2023
Early initiation of B-vitamin supplementation may reduce symptoms and explain intrafamilial variability: Insights from two sibling pairs from the TANGO2 natural history studyChristina Y Miyake, Saad A Ehsan, Lilei Zhang, et al.
Journal of Medical Genetics|January 19, 2021
Clinical exome sequencing data reveal high diagnostic yields for congenital diaphragmatic hernia plus (CDH+) and new phenotypic expansions involving CDHTiana M Scott, Ian M Campbell, Andres Hernandez-Garcia, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
Clinical geneticists' views of VACTERL/VATER associationBenjamin D Solomon, Kelly A Bear, Virginia Kimonis, et al.
Stem Cell Reports|September 26, 2017
SOX7 Is Required for Muscle Satellite Cell Development and MaintenanceRashida F Rajgara, Neena Lala-Tabbert, François Marchildon, et al.
Pageof 13

Showing results (21-30 of 128) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics. Part A|July 7, 2022
Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic herniaYoel Gofin, Xiaonan Zhao, Amanda Gerard, et al.
American Journal of Medical Genetics. Part A|July 17, 2009
A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorderJaime M Williams, Tyler F Beck, David M Pearson, et al.
Development (Cambridge, England)|June 28, 2015
Stromal Fat4 acts non-autonomously with Dchs1/2 to restrict the nephron progenitor poolMazdak Bagherie-Lachidan, Antoine Reginensi, Qun Pan, et al.
Human Molecular Genetics|March 27, 2021
RERE deficiency contributes to the development of orofacial clefts in humans and miceBum Jun Kim, Hitisha P Zaveri, Peter N Kundert, et al.
Plos One|April 18, 2017
Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disabilityChristina Grau, Molly Starkovich, Mahshid S Azamian, et al.
European Journal of Human Genetics : EJHG|September 5, 2025
Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+)E Andres Rivera-Munoz, Xiaonan E Zhao, Jill A Rosenfeld, et al.
American Journal of Medical Genetics. Part A|July 8, 2023
Early initiation of B-vitamin supplementation may reduce symptoms and explain intrafamilial variability: Insights from two sibling pairs from the TANGO2 natural history studyChristina Y Miyake, Saad A Ehsan, Lilei Zhang, et al.
Journal of Medical Genetics|January 19, 2021
Clinical exome sequencing data reveal high diagnostic yields for congenital diaphragmatic hernia plus (CDH+) and new phenotypic expansions involving CDHTiana M Scott, Ian M Campbell, Andres Hernandez-Garcia, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
Clinical geneticists' views of VACTERL/VATER associationBenjamin D Solomon, Kelly A Bear, Virginia Kimonis, et al.
Stem Cell Reports|September 26, 2017
SOX7 Is Required for Muscle Satellite Cell Development and MaintenanceRashida F Rajgara, Neena Lala-Tabbert, François Marchildon, et al.
Pageof 13