Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Selena L. Tran"'
Autor:
Carole A. Samango-Sprouse, Austin P. Gillies, Andrea L. Gropman, Patricia Hendrie, Grace F. Porter, Francie L. Mitchell, Laura L. Tosi, Patricia C. Lasutschinkow, Selena L. Tran, Leigh Ruland, Elmer N. Rajah, Rick Peret, Teresa Sadeghin
Publikováno v:
American Journal of Medical Genetics Part A. 185:3531-3540
49,XXXXY is the rarest X and Y chromosomal variation, with an incidence of 1 in 80,000-100,000 live male births and has been associated with numerous musculoskeletal abnormalities. Data was collected from an international cohort of boys with 49,XXXXY
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f7e827e9c7ee45ac1d84713da6d9a6b
https://doi.org/10.1002/ajmg.a.61578
https://doi.org/10.1002/ajmg.a.61578
Autor:
Andrea L. Gropman, Carole A. Samango-Sprouse, Teresa Sadeghin, Patricia C. Lasutschinkow, Selena L. Tran, Grace F. Porter
Publikováno v:
Prenatal Diagnosis. 40:470-480
Objective To investigate the attitudes of parents of children with a sex chromosome aneuploidy (SCA) regarding the impact of an early diagnosis and noninvasive prenatal testing (NIPT). Method A survey consisting of multiple choice and long response f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56337b2fb9b95ef17d7e93a24f1a13bd
https://doi.org/10.1002/pd.5580
https://doi.org/10.1002/pd.5580
Autor:
Andrea L. Gropman, Teresa Sadeghin, Carole A. Samango-Sprouse, Sherida Powell, Selena L. Tran
Publikováno v:
American Journal of Medical Genetics Part A. 179:2374-2381
This cross-sectional, retrospective analysis investigated the possible effect of hormonal replacement therapy (HRT) on working memory (WM) and competency/adaptive functioning (CAF) in boys with 47,XXY; the effect of timing of 47,XXY diagnosis on thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78b600316048107224439e7f43232c70
https://doi.org/10.1002/ajmg.a.61360
https://doi.org/10.1002/ajmg.a.61360
Autor:
Patricia C. Lasutschinkow, Selena L. Tran, Andrea L. Gropman, Carole A. Samango-Sprouse, Grace F. Porter, Debra R Counts
Publikováno v:
The Application of Clinical Genetics. 12:191-202
47,XXY (Klinefelter syndrome [KS]) is the most common sex chromosomal aneuploidy (1:660), yet, despite this, only 25% of the males are ever diagnosed. Males with 47,XXY present with characteristic symptoms throughout their lifetime with typical physi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09d71a0e58dc288924b7eb0e6ab67c03
https://doi.org/10.2147/tacg.s180450
https://doi.org/10.2147/tacg.s180450
Autor:
Sherida Powell, Carole A. Samango-Sprouse, Francie L. Mitchell, Teresa Sadeghin, Andrea L. Gropman, Patricia C. Lasutschinkow, Selena L. Tran
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 182(8)
This cross-sectional study examined the neurodevelopment of a large, prenatally diagnosed population of boys with 47,XXY; investigated the potentially positive effects of early hormonal therapy (EHT) on language, cognition, and motor in this populati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::caf8a9f2ada1bb3aa1889c188980568f
https://pubmed.ncbi.nlm.nih.gov/32220052
https://pubmed.ncbi.nlm.nih.gov/32220052