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Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2.

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Title: Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2.
Authors: Morison LD; Speech and Language, Murdoch Children's Research Institute, Parkville, Victoria, Australia.; Department of Audiology and Speech Pathology, The University of Melbourne, Parkville, Victoria, Australia., Braden R; Speech and Language, Murdoch Children's Research Institute, Parkville, Victoria, Australia.; Department of Audiology and Speech Pathology, The University of Melbourne, Parkville, Victoria, Australia., Amor DJ; Speech and Language, Murdoch Children's Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, The University of Melbourne, Parkville, Victoria, Australia.; Department of Paediatrics, the Royal Children's Hospital, Parkville, Victoria, Australia., Morgan AT; Speech and Language, Murdoch Children's Research Institute, Parkville, Victoria, Australia.; Department of Audiology and Speech Pathology, The University of Melbourne, Parkville, Victoria, Australia.; Department of Paediatrics, the Royal Children's Hospital, Parkville, Victoria, Australia.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2025 Dec; Vol. 197 (12), pp. e64190. Date of Electronic Publication: 2025 Jul 26.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2.
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  Data: <searchLink fieldCode="AU" term="%22Morison+LD%22">Morison LD</searchLink>; Speech and Language, Murdoch Children's Research Institute, Parkville, Victoria, Australia.; Department of Audiology and Speech Pathology, The University of Melbourne, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Braden+R%22">Braden R</searchLink>; Speech and Language, Murdoch Children's Research Institute, Parkville, Victoria, Australia.; Department of Audiology and Speech Pathology, The University of Melbourne, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Amor+DJ%22">Amor DJ</searchLink>; Speech and Language, Murdoch Children's Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, The University of Melbourne, Parkville, Victoria, Australia.; Department of Paediatrics, the Royal Children's Hospital, Parkville, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Morgan+AT%22">Morgan AT</searchLink>; Speech and Language, Murdoch Children's Research Institute, Parkville, Victoria, Australia.; Department of Audiology and Speech Pathology, The University of Melbourne, Parkville, Victoria, Australia.; Department of Paediatrics, the Royal Children's Hospital, Parkville, Victoria, Australia.
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  Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2025 Dec; Vol. 197 (12), pp. e64190. <i>Date of Electronic Publication: </i>2025 Jul 26.
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        Value: 10.1002/ajmg.a.64190
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              Text: 2025 Dec
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