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Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel Cases.
Katz, Olivia L; Wild, K Taylor; McEldrew, Deborah; Kaur, Maninder; Raible, Sarah; Skraban, Cara M; Zackai, Elaine H; Medne, Livija; Izumi, Kosuke; Fortunato, Sierra; Weatherly, Jamila; Hartman, Tiffiney; Deppen, Paul; Blair, Justin; Devkota, Batsal; Schindler, Emma; Hedrick, Holly L; Peranteau, William; Krantz, Ian D.
Afiliação
  • Katz OL; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Wild KT; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA; Division of Neonatology, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • McEldrew D; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Kaur M; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Raible S; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Skraban CM; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Zackai EH; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Medne L; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Izumi K; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Fortunato S; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Weatherly J; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Hartman T; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Deppen P; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Blair J; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Devkota B; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA; Department of Biomedical and Health Informatics, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Schindler E; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA.
  • Hedrick HL; Center for Fetal Research, The Children's Hospital of Philadelphia, Philadelphia, PA; Department of Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Peranteau W; Center for Fetal Research, The Children's Hospital of Philadelphia, Philadelphia, PA; Department of Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Krantz ID; Division of Human Genetics, Roberts Individualized Medical Genetics Center, The Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA. Electronic address: krantz@chop.edu.
J Pediatr ; 246: 251-265.e2, 2022 07.
Article em En | MEDLINE | ID: mdl-35314152
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hérnias Diafragmáticas Congênitas Tipo de estudo: Etiology_studies Limite: Humans / Newborn Idioma: En Revista: J Pediatr Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hérnias Diafragmáticas Congênitas Tipo de estudo: Etiology_studies Limite: Humans / Newborn Idioma: En Revista: J Pediatr Ano de publicação: 2022 Tipo de documento: Article