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Autor:
Jozef Gecz, Denise Horn, Sherindan O'Donnell, Marie Shaw, Neva H. Malek, Nicole Bain, Kerry Fagan, Trent Burgess, Christopher W. Carr, Anna K. Le Fevre, Sharelle Taylor, Omar A. Abdul-Rahman, Matthew F. Hunter
Publikováno v:
American Journal of Medical Genetics Part A. 161:3166-3175
Mutations in FOXP1, located at 3p13, have been reported in patients with global developmental delay (GDD), intellectual disability (ID), and speech defects. Mutations in FOXP2, located at 7q31, are well known to cause developmental speech and languag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8a25143d5ebeec8d8e25b8daf360dd0
https://doi.org/10.1002/ajmg.a.36174
https://doi.org/10.1002/ajmg.a.36174
