Showing results (21-30 of 27) with videos related to
Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
European Journal of Endocrinology|October 17, 2018
Noonan syndrome males display Sertoli cell-specific primary testicular insufficiencySophie Moniez, Catherine Pienkowski, Benoit Lepage, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2021
SNORD116 and growth hormone therapy impact IGFBP7 in Prader-Willi syndromeSanaa Eddiry, Gwenaelle Diene, Catherine Molinas, et al.Pediatrics|January 20, 2017
The Use of Oxytocin to Improve Feeding and Social Skills in Infants With Prader-Willi SyndromeMaïthé Tauber, Kader Boulanouar, Gwenaelle Diene, et al.American Journal of Medical Genetics. Part A|May 1, 2014
New candidate loci identified by array-CGH in a cohort of 100 children presenting with syndromic obesityMarie-Laure Vuillaume, Sophie Naudion, Guillaume Banneau, et al.Clinical Epigenetics|November 8, 2022
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disordersDeborah Mackay, Jet Bliek, Masayo Kagami, et al.Annales D'Endocrinologie|March 21, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditionsLaurence Faivre, Camille Level, Régis Coutant, et al.Annales D'Endocrinologie|May 8, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditionsLaurence Faivre, Camille Level, Régis Coutant, et al.Pageof 3