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. |
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| 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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