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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 28, 2022
A longitudinal perspective of hormone replacement therapies (HRTs) on neuromotor capabilities in males with 47,XXY (Klinefelter syndrome)Carole Samango-Sprouse, Michaela Reiko Brooks, Debra Counts, et al.Journal of the National Cancer Institute. Monographs|March 24, 2005
Preimplantation genetic diagnosis (PGD) for heritable neoplasiaJoe Leigh Simpson, Sandra A Carson, Pauline CisnerosFrontiers in Endocrinology|January 5, 2026
Case Report: An exploration of the neurodevelopmental phenotype of five patients with 48,XXYY during early childhood yearsMargaret Olaya, Carole Samango-Sprouse, Debra Counts, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 30, 2023
Reading skills in males with 47,XXY: Risk factors and the influence of hormonal replacement therapy (HRT)Michaela R Brooks, Andrea L Gropman, Mary P Hamzik, et al.Prenatal Diagnosis|April 3, 2012
Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trialRonald J Wapner, Deborah A Driscoll, Joe Leigh SimpsonReproductive Biomedicine Online|September 30, 2006
Recovery and amplification of placental RNA from dried maternal blood spots: utility for non-invasive prenatal diagnosisCarolina J Jorgez, Joe Leigh Simpson, Farideh Z BischoffFertility and Sterility|May 13, 2006
Professional self-regulation for preimplantation genetic diagnosis: experience of the American Society for Reproductive Medicine and other professional societiesJoe Leigh Simpson, Robert W Rebar, Sandra Ann CarsonHuman Reproduction Update|December 1, 2004
Cell-free fetal DNA in maternal blood: kinetics, source and structureFarideh Z Bischoff, Dorothy E Lewis, Joe Leigh SimpsonPlos One|August 12, 2016
Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing PopulationCarole Samango-Sprouse, Eser Kırkızlar, Megan P Hall, et al.Frontiers in Endocrinology|November 3, 2025
First description of co-occurrence of 49,XXXXY and X-linked Cornelia de Lange syndrome: case reportSumaiya Al-Rashdi, Lori Ekstrom, Aedin Collins, et al.Pageof 13