Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Aaliya A. Ahmad"'
Publikováno v:
Clinical Case Reports, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract Haploinsufficiency of FOXP2 causes FOXP2‐related speech and language disorder. We report a 9.8 Mb deletion downstream of FOXP2 in a girl with speech and language impairment, developmental delay, and other features. We propose involvement o
Externí odkaz:
https://doaj.org/article/77d50c063b0b46d3961b42ee28e434f6
Autor:
Ahmad A; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA., Fitzgerald-Butt SM; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA., Ware SM; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA.; Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA., Ison HE; Stanford Center for Inherited Cardiovascular Disease, Stanford Health Care, Stanford, California, USA., Elmore LR; Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA., Helm BM; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA.; Department of Epidemiology, Indiana University Fairbanks School of Public Health, Indianapolis, Indiana, USA.
Publikováno v:
Journal of genetic counseling [J Genet Couns] 2022 Jun; Vol. 31 (3), pp. 735-745. Date of Electronic Publication: 2021 Dec 07.