Your browser doesn't support javascript.
loading
Androgenetic chimerism as an etiology for Beckwith-Wiedemann syndrome: diagnosis and management.
Sheppard, Sarah E; Lalonde, Emilie; Adzick, N Scott; Beck, Anita E; Bhatti, Tricia; De Leon, Diva D; Duffy, Kelly A; Ganguly, Arupa; Hathaway, Evan; Ji, Jianling; Linn, Rebecca; Lord, Katherine; Randolph, Linda M; Sajorda, Brian; States, Lisa; Conlin, Laura K; Kalish, Jennifer M.
Afiliação
  • Sheppard SE; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Lalonde E; Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Adzick NS; Department of Pathology and Laboratory Medicine, University of Pennsylvania Health System, Philadelphia, PA, USA.
  • Beck AE; Department of Surgery, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Bhatti T; Department of Pediatrics, Division of Genetic Medicine, University of Washington & Seattle Children's Hospital, Seattle, WA, USA.
  • De Leon DD; Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Duffy KA; Division of Endocrinology and Diabetes, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Ganguly A; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Hathaway E; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Ji J; Department of Pathology and Laboratory Medicine, University of Pennsylvania Health System, Philadelphia, PA, USA.
  • Linn R; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Lord K; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Randolph LM; Center for Personalized Medicine, Department of Pathology & Laboratory Medicine, Children's Hospital Los Angeles, and Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
  • Sajorda B; Department of Pathology and Laboratory Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • States L; Division of Endocrinology and Diabetes, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Conlin LK; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Kalish JM; Division of Medical Genetics, Department of Pediatrics, Children's Hospital Los Angeles and Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Genet Med ; 21(11): 2644-2649, 2019 11.
Article em En | MEDLINE | ID: mdl-31147633
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Beckwith-Wiedemann / Dissomia Uniparental Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Beckwith-Wiedemann / Dissomia Uniparental Idioma: En Ano de publicação: 2019 Tipo de documento: Article