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Myhre syndrome: A first familial recurrence and broadening of the phenotypic spectrum.

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Title: Myhre syndrome: A first familial recurrence and broadening of the phenotypic spectrum.
Authors: Meerschaut I; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Department of Pediatrics, Ghent University Hospital, Ghent, Belgium., Beyens A; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Department of Dermatology, Ghent University Hospital, Ghent, Belgium., Steyaert W; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium., De Rycke R; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.; VIB Center for Inflammation Research, Ghent, Belgium.; Ghent University Expertise Centre for Transmission Electron Microscopy and VIB Bioimaging Core, Ghent, Belgium., Bonte K; Department of Head, Neck and Maxillofacial Surgery, Ghent University Hospital, Ghent, Belgium., De Backer T; Department of Cardiology, Ghent University Hospital, Ghent, Belgium., Janssens S; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium., Panzer J; Department of Pediatric Cardiology, Ghent University Hospital, Ghent, Belgium., Plasschaert F; Department of Orthopedic Surgery, Ghent University Hospital, Ghent, Belgium., De Wolf D; Department of Pediatric Cardiology, Ghent University Hospital, Ghent, Belgium., Callewaert B; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2019 Dec; Vol. 179 (12), pp. 2494-2499. Date of Electronic Publication: 2019 Oct 09.
Publication Type: Case Reports; 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: Myhre syndrome: A first familial recurrence and broadening of the phenotypic spectrum.
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  Data: <searchLink fieldCode="AU" term="%22Meerschaut+I%22">Meerschaut I</searchLink>; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Department of Pediatrics, Ghent University Hospital, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Beyens+A%22">Beyens A</searchLink>; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Department of Dermatology, Ghent University Hospital, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Steyaert+W%22">Steyaert W</searchLink>; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22De+Rycke+R%22">De Rycke R</searchLink>; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.; VIB Center for Inflammation Research, Ghent, Belgium.; Ghent University Expertise Centre for Transmission Electron Microscopy and VIB Bioimaging Core, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Bonte+K%22">Bonte K</searchLink>; Department of Head, Neck and Maxillofacial Surgery, Ghent University Hospital, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22De+Backer+T%22">De Backer T</searchLink>; Department of Cardiology, Ghent University Hospital, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Janssens+S%22">Janssens S</searchLink>; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Panzer+J%22">Panzer J</searchLink>; Department of Pediatric Cardiology, Ghent University Hospital, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Plasschaert+F%22">Plasschaert F</searchLink>; Department of Orthopedic Surgery, Ghent University Hospital, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22De+Wolf+D%22">De Wolf D</searchLink>; Department of Pediatric Cardiology, Ghent University Hospital, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Callewaert+B%22">Callewaert B</searchLink>; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
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  Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2019 Dec; Vol. 179 (12), pp. 2494-2499. <i>Date of Electronic Publication: </i>2019 Oct 09.
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  Data: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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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>101235741 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1552-4833 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215524825%22">15524825 </searchLink><i>NLM ISO Abbreviation: </i>Am J Med Genet A <i>Subsets: </i>MEDLINE
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        Value: 10.1002/ajmg.a.61377
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              Text: 2019 Dec
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