Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Rick Peret"'
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:
Emily Stapleton, Rick Peret, Francie L. Mitchell, Laura L. Tosi, Kathryn Haskell, Courtney Sprouse, Carole A. Samango-Sprouse, Andrea L. Gropman, Teresa Sadeghin
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 163:44-49
49, XXXXY is a rare aneuploidy and variant of Klinefelter syndrome, occurring in 1 per 80,000-100,000 live births. We present a cohort of 40 affected males, focusing on musculoskeletal problems. Subjects were participants in an annual 49er family sup
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::609900021ed3b6dbbfc77f49ac0d45f1
https://doi.org/10.1002/ajmg.c.31354
https://doi.org/10.1002/ajmg.c.31354