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Frontometaphyseal dysplasia and keloid formation without FLNA mutations.
Basart, Hanneke; van de Kar, Annekatrien; Adès, Lesley; Cho, Tae-Joon; Carter, Erin; Maas, Saskia M; Wilson, Louise C; van der Horst, Chantal M A M; Wade, Emma M; Robertson, Stephen P; Hennekam, Raoul C.
Affiliation
  • Basart H; Department of Pediatrics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • van de Kar A; Department of Plastic and Reconstructive Surgery, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Adès L; Department of Plastic and Reconstructive Surgery, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Cho TJ; Discipline of Pediatrics and Child Health, Department of Clinical Genetics, University of Sydney, The Children's Hospital, Westmead, Sydney, Australia.
  • Carter E; Division of Pediatric Orthopedics, Seoul National University Children's Hospital, Seoul, Republic of Korea.
  • Maas SM; Kathryn O. and Alan C. Greenberg Center for Skeletal Dysplasias, Hospital for Special Surgery, New York, New York.
  • Wilson LC; Department of Pediatrics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • van der Horst CM; Clinical Genetics Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Wade EM; Department of Plastic and Reconstructive Surgery, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Robertson SP; Department of Women's and Children's Health, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
  • Hennekam RC; Department of Women's and Children's Health, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
Am J Med Genet A ; 167(6): 1215-22, 2015 Jun.
Article in En | MEDLINE | ID: mdl-25899317
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteochondrodysplasias / Pierre Robin Syndrome / Tracheal Stenosis / Cleft Palate / Forehead / Keloid / Intellectual Disability Limits: Adolescent / Child / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2015 Document type: Article Affiliation country:
Fulltext
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Print
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteochondrodysplasias / Pierre Robin Syndrome / Tracheal Stenosis / Cleft Palate / Forehead / Keloid / Intellectual Disability Limits: Adolescent / Child / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2015 Document type: Article Affiliation country: