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. |
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| 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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| ISSN: | 1552-4833 |
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| DOI: | 10.1002/ajmg.a.64190 |
