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ASXL3-related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism.

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Title: ASXL3-related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism.
Authors: Woods E; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield, UK.; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK., Holmes N; Sheffield Diagnostic Genetics Service, Sheffield Children's Hospital, Sheffield, UK., Albaba S; Sheffield Diagnostic Genetics Service, Sheffield Children's Hospital, Sheffield, UK., Evans IR; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.; The Bateson Centre, University of Sheffield, Sheffield, UK., Balasubramanian M; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield, UK.; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.; The Bateson Centre, University of Sheffield, Sheffield, UK.
Source: Clinical genetics [Clin Genet] 2024 May; Vol. 105 (5), pp. 470-487. Date of Electronic Publication: 2024 Feb 29.
Publication Type: Journal Article; Review
Journal Info: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: <searchLink fieldCode="AU" term="%22Woods+E%22">Woods E</searchLink>; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield, UK.; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.<br /><searchLink fieldCode="AU" term="%22Holmes+N%22">Holmes N</searchLink>; Sheffield Diagnostic Genetics Service, Sheffield Children's Hospital, Sheffield, UK.<br /><searchLink fieldCode="AU" term="%22Albaba+S%22">Albaba S</searchLink>; Sheffield Diagnostic Genetics Service, Sheffield Children's Hospital, Sheffield, UK.<br /><searchLink fieldCode="AU" term="%22Evans+IR%22">Evans IR</searchLink>; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.; The Bateson Centre, University of Sheffield, Sheffield, UK.<br /><searchLink fieldCode="AU" term="%22Balasubramanian+M%22">Balasubramanian M</searchLink>; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield, UK.; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.; The Bateson Centre, University of Sheffield, Sheffield, UK.
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  Data: <searchLink fieldCode="JN" term="%220253664%22">Clinical genetics</searchLink> [Clin Genet] 2024 May; Vol. 105 (5), pp. 470-487. <i>Date of Electronic Publication: </i>2024 Feb 29.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Munksgaard%22">Munksgaard </searchLink><i>Country of Publication: </i>Denmark <i>NLM ID: </i>0253664 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1399-0004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200099163%22">00099163 </searchLink><i>NLM ISO Abbreviation: </i>Clin Genet <i>Subsets: </i>MEDLINE
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        Value: 10.1111/cge.14506
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      – Code: eng
        Text: English
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              Text: 2024 May
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