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Characterization of the Beckwith-Wiedemann spectrum: Diagnosis and management.
Duffy, Kelly A; Cielo, Christopher M; Cohen, Jennifer L; Gonzalez-Gandolfi, Christina X; Griff, Jessica R; Hathaway, Evan R; Kupa, Jonida; Taylor, Jesse A; Wang, Kathleen H; Ganguly, Arupa; Deardorff, Matthew A; Kalish, Jennifer M.
Afiliación
  • Duffy KA; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Cielo CM; Division of Pulmonary Medicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Cohen JL; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Gonzalez-Gandolfi CX; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Griff JR; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Hathaway ER; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Kupa J; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Taylor JA; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Wang KH; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Ganguly A; Division of Plastic and Reconstructive Surgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Deardorff MA; Department of Surgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Kalish JM; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Am J Med Genet C Semin Med Genet ; 181(4): 693-708, 2019 12.
Article en En | MEDLINE | ID: mdl-31469230
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Beckwith-Wiedemann Tipo de estudio: Diagnostic_studies / Guideline Límite: Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet C Semin Med Genet Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article
Texto completo
Añadir a Mi BVS
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Beckwith-Wiedemann Tipo de estudio: Diagnostic_studies / Guideline Límite: Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet C Semin Med Genet Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article