Showing results (411-420 of 908) with videos related to

Sort By:
Pageof 91
Molecular Genetics and Metabolism|December 19, 2018
Cryptic intronic NBAS variant reveals the genetic basis of recurrent liver failure in a childRocio Rius, Lisa G Riley, Yiran Guo, et al.
Neuropsychology|January 19, 2012
Age group and sex differences in performance on a computerized neurocognitive battery in children age 8-21Ruben C Gur, Jan Richard, Monica E Calkins, et al.
Scientific Reports|January 18, 2023
Molecular diagnosis and novel genes and phenotypes in a pediatric thoracic insufficiency cohortAlanna Strong, Meckenzie Behr, Carina Lott, et al.
Clinical and Translational Gastroenterology|March 8, 2018
Food allergen triggers are increased in children with the TSLP risk allele and eosinophilic esophagitisLisa M Fahey, Prasanna M Chandramouleeswaran, Shaobo Guan, et al.
Blood|February 11, 2021
RUNX-1 haploinsufficiency causes a marked deficiency of megakaryocyte-biased hematopoietic progenitor cellsBrian Estevez, Sara Borst, Danuta Jarocha, et al.
American Journal of Medical Genetics. Part A|May 7, 2021
A new syndrome of moyamoya disease, kidney dysplasia, aminotransferase elevation, and skin disease associated with de novo variants in RNF213Alanna Strong, Gina O'Grady, Evelyn Shih, et al.
Plos One|June 4, 2010
Common variation in ISL1 confers genetic susceptibility for human congenital heart diseaseKristen N Stevens, Hakon Hakonarson, Cecilia E Kim, et al.
Science Immunology|October 24, 2020
A distinct GM-CSF+ T helper cell subset requires T-bet to adopt a TH1 phenotype and promote neuroinflammationJavad Rasouli, Giacomo Casella, Satoshi Yoshimura, et al.
Journal of Pediatric Urology|May 8, 2025
Genetic analysis of two bladder exstrophy populations of South Asian and North American originJohn K Weaver, Dana A Weiss, Austin Thompson, et al.
Pageof 91