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Hearing, Speech, Language, and Communicative Participation in Patients With Apert Syndrome: Analysis of Correlation With Fibroblast Growth Factor Receptor 2 Mutation.

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Title: Hearing, Speech, Language, and Communicative Participation in Patients With Apert Syndrome: Analysis of Correlation With Fibroblast Growth Factor Receptor 2 Mutation.
Authors: Kilcoyne S; Oxford Craniofacial Unit., Luscombe C; Oxford Craniofacial Unit., Scully P; Department of Audiology., Overton S; Oxford Craniofacial Unit., Brockbank S; Oxford Craniofacial Unit., Swan MC; Spires Cleft Centre, Oxford University Hospitals NHS Foundation Trust., Johnson D; Oxford Craniofacial Unit., Wall S; Oxford Craniofacial Unit., Wilkie AOM; Oxford Craniofacial Unit.; MRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom.
Source: The Journal of craniofacial surgery [J Craniofac Surg] 2022 Jan-Feb 01; Vol. 33 (1), pp. 243-250.
Publication Type: Journal Article
Journal Info: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 9010410 Publication Model: Print Cited Medium: Internet ISSN: 1536-3732 (Electronic) Linking ISSN: 10492275 NLM ISO Abbreviation: J Craniofac Surg
Database: MEDLINE Ultimate
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  Data: Hearing, Speech, Language, and Communicative Participation in Patients With Apert Syndrome: Analysis of Correlation With Fibroblast Growth Factor Receptor 2 Mutation.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Lippincott+Williams+%26+Wilkins%22">Lippincott Williams & Wilkins </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9010410 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1536-3732 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210492275%22">10492275 </searchLink><i>NLM ISO Abbreviation: </i>J Craniofac Surg
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        Value: 10.1097/SCS.0000000000008019
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        Text: English
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        StartPage: 243
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      – TitleFull: Hearing, Speech, Language, and Communicative Participation in Patients With Apert Syndrome: Analysis of Correlation With Fibroblast Growth Factor Receptor 2 Mutation.
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              Text: 2022 Jan-Feb 01
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              Y: 2022
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