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Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2016
Family health history reporting is sensitive to small changes in wordingLiam S Conway-Pearson, Kurt D Christensen, Sarah K Savage, et al.European Journal of Human Genetics : EJHG|June 11, 2015
STAG3 truncating variant as the cause of primary ovarian insufficiencyPolona Le Quesne Stabej, Hywel J Williams, Chela James, et al.Endocrine Connections|July 14, 2026
External validation of the PASO prediction score for primary aldosteronismAlaa Abdelsalam, Mohammad Mahmoud Rajab Eddama, Virginia Rozalen-Garcia, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|October 27, 2025
Longitudinal modeling of upper extremity function in multiple sclerosis: Associations for clinical and sociodemographic factorsFarren Bs Briggs, Jiayue Yang, Karlo Toljan, et al.Dalton Transactions (Cambridge, England : 2003)|November 4, 2024
Cyrene™ as a green alternative to N,N'-dimethylformamide (DMF) in the synthesis of MLCT-emissive ruthenium(II) polypyridyl complexes for biological applicationsSteffan D James, Christopher E Elgar, Dandan Chen, et al.Journal of the Endocrine Society|November 21, 2019
Next-Generation Sequencing Reveals Novel Genetic Variants (SRY, DMRT1, NR5A1, DHH, DHX37) in Adults With 46,XY DSDFederica Buonocore, Oliver Clifford-Mobley, Tom F J King, et al.Neurology|January 21, 2021
Brain Histopathology of Adult Decedents After Extracorporeal Membrane OxygenationImad R Khan, Yang Gu, Benjamin P George, et al.The Journal of Clinical Endocrinology and Metabolism|April 16, 2013
A long-acting human growth hormone with delayed clearance (VRS-317): results of a double-blind, placebo-controlled, single ascending dose study in growth hormone-deficient adultsKevin C J Yuen, Gerard S Conway, Vera Popovic, et al.The Journal of Clinical Endocrinology and Metabolism|October 2, 2018
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice GuidelinePhyllis W Speiser, Wiebke Arlt, Richard J Auchus, et al.Clinical Endocrinology|September 5, 2001
Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterizationR Quinton, V M Duke, A Robertson, et al.Pageof 40