Showing results (61-70 of 72) with videos related to

Sort By:
Pageof 8
Journal of Medical Genetics|October 13, 2023
Intellectual disability syndrome associated with a homozygous founder variant in SGSM3 in Ashkenazi JewsRivka Birnbaum, Shlomit Ezer, Nava Shaul Lotan, et al.
BMC Infectious Diseases|January 6, 2016
Development of the Flu-PRO: a patient-reported outcome (PRO) instrument to evaluate symptoms of influenzaJohn H Powers, M Lourdes Guerrero, Nancy Kline Leidy, et al.
Nature Communications|July 13, 2023
Cytochrome c lysine acetylation regulates cellular respiration and cell death in ischemic skeletal musclePaul T Morse, Gonzalo Pérez-Mejías, Junmei Wan, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 29, 2024
The thermoneutral zone in women takes an "arctic" shift compared to menRobert J Brychta, Suzanne McGehee, Shan Huang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 18, 2018
Correction: TANGO2: expanding the clinical phenotype and spectrum of pathogenic variantsJennifer N Dines, Katie Golden-Grant, Amy LaCroix, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research|February 26, 2018
Reliability, Validity, and Responsiveness of InFLUenza Patient-Reported Outcome (FLU-PRO©) Scores in Influenza-Positive PatientsJohn H Powers, Elizabeth D Bacci, M Lourdes Guerrero, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2018
TANGO2: expanding the clinical phenotype and spectrum of pathogenic variantsJennifer N Dines, Katie Golden-Grant, Amy LaCroix, et al.
American Journal of Medical Genetics. Part A|May 25, 2019
Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic featuresElliot S Stolerman, Elizabeth Francisco, Jennifer L Stallworth, et al.
American Journal of Human Genetics|October 4, 2016
De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical PhenotypeVandana Shashi, Loren D M Pena, Katherine Kim, et al.
HGG Advances|November 21, 2022
A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorderLot Snijders Blok, Jolijn Verseput, Dmitrijs Rots, et al.
Pageof 8