Showing results (11-20 of 26) with videos related to
Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|April 10, 2014
Expanding the phenotypic profile of boys with 47, XXY: the impact of familial learning disabilitiesCarole A Samango-Sprouse, Emily J Stapleton, Francie L Mitchell, et al.Prenatal Diagnosis|October 30, 2019
Impact of early diagnosis and noninvasive prenatal testing (NIPT): Knowledge, attitudes, and experiences of parents of children with sex chromosome aneuploidies (SCAs)Carole A Samango-Sprouse, Grace F Porter, Patricia C Lasutschinkow, et al.The Application of Clinical Genetics|November 8, 2019
Update On The Clinical Perspectives And Care Of The Child With 47,XXY (Klinefelter Syndrome)Carole A Samango-Sprouse, Debra R Counts, Selena L Tran, et al.American Journal of Medical Genetics. Part A|March 29, 2020
Neurodevelopmental outcome of prenatally diagnosed boys with 47,XXY (Klinefelter syndrome) and the potential influence of early hormonal therapyCarole A Samango-Sprouse, Selena L Tran, Patricia C Lasutschinkow, et al.American Journal of Medical Genetics. Part A|July 15, 2020
Neurocognitive development and capabilities in boys with 49,XXXXY syndromeAndrea L Gropman, Grace F Porter, Patricia C Lasutschinkow, et al.American Journal of Medical Genetics. Part A|July 30, 2020
Speech and language development in children with 49,XXXXY syndromeCarole A Samango-Sprouse, Patricia C Lasutschinkow, Michael McLeod, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2023
The behavioral profile of 49,XXXXY and the potential impact of testosterone replacement therapyCarole A Samango-Sprouse, Mary P Hamzik, Eliana Gropman, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 30, 2013
Musculoskeletal anomalies in a large cohort of boys with 49, XXXXYCourtney Sprouse, Laura Tosi, Emily Stapleton, et al.American Journal of Medical Genetics. Part A|May 27, 2010
Clinical variability and novel neurodevelopmental findings in 49, XXXXY syndromeAndrea L Gropman, Alan Rogol, Ilene Fennoy, et al.Frontiers in Pediatrics|April 4, 2022
Case Report: A Case Study on the Neurodevelopmental Profile of a Child With Pallister-Killian Syndrome and His Unaffected TwinCarole A Samango-Sprouse, Mary P Hamzik, Kenneth Rosenbaum, et al.Pageof 3