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PRC2-complex related dysfunction in overgrowth syndromes: A review of EZH2, EED, and SUZ12 and their syndromic phenotypes.

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Title: PRC2-complex related dysfunction in overgrowth syndromes: A review of EZH2, EED, and SUZ12 and their syndromic phenotypes.
Authors: Cyrus S; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada., Burkardt D; Center for Human Genetics, University Hospitals Rainbow Babies and Children/Department of Genetics, Case Western Reserve University, Cleveland, Ohio., Weaver DD; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana., Gibson WT; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.; British Columbia Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
Source: American journal of medical genetics. Part C, Seminars in medical genetics [Am J Med Genet C Semin Med Genet] 2019 Dec; Vol. 181 (4), pp. 519-531. Date of Electronic Publication: 2019 Nov 14.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235745 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4876 (Electronic) Linking ISSN: 15524868 NLM ISO Abbreviation: Am J Med Genet C Semin Med Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: PRC2-complex related dysfunction in overgrowth syndromes: A review of EZH2, EED, and SUZ12 and their syndromic phenotypes.
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  Data: <searchLink fieldCode="AU" term="%22Cyrus+S%22">Cyrus S</searchLink>; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.<br /><searchLink fieldCode="AU" term="%22Burkardt+D%22">Burkardt D</searchLink>; Center for Human Genetics, University Hospitals Rainbow Babies and Children/Department of Genetics, Case Western Reserve University, Cleveland, Ohio.<br /><searchLink fieldCode="AU" term="%22Weaver+DD%22">Weaver DD</searchLink>; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.<br /><searchLink fieldCode="AU" term="%22Gibson+WT%22">Gibson WT</searchLink>; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.; British Columbia Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
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  Data: <searchLink fieldCode="JN" term="%22101235745%22">American journal of medical genetics. Part C, Seminars in medical genetics</searchLink> [Am J Med Genet C Semin Med Genet] 2019 Dec; Vol. 181 (4), pp. 519-531. <i>Date of Electronic Publication: </i>2019 Nov 14.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101235745 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1552-4876 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215524868%22">15524868 </searchLink><i>NLM ISO Abbreviation: </i>Am J Med Genet C Semin Med Genet <i>Subsets: </i>MEDLINE
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        Value: 10.1002/ajmg.c.31754
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      – Code: eng
        Text: English
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        StartPage: 519
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      – TitleFull: PRC2-complex related dysfunction in overgrowth syndromes: A review of EZH2, EED, and SUZ12 and their syndromic phenotypes.
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              Text: 2019 Dec
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