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Extending the prenatal Noonan's phenotype by review of ultrasound and autopsy data.
Lamouroux, Audrey; Dauge, Coralie; Wells, Constance; Mousty, Eve; Pinson, Lucile; Cavé, Hélène; Capri, Yline; Faure, Jean-Michel; Grosjean, Frédéric; Sauvestre, Fanny; Attié-Bitach, Tania; Pelluard, Fanny; Geneviève, David.
Afiliação
  • Lamouroux A; Clinical Genetics Department, Montpellier University Hospital, University of Montpellier, Montpellier, France.
  • Dauge C; Obstetrical Gynecology Department, Nîmes University Hospital, University of Montpellier, Nîmes, France.
  • Wells C; Charles Coulomb Laboratory, UMR 5221 CNRS-UM, BNIF User Facility Imaging, University of Montpellier, CNRS, Montpellier, France.
  • Mousty E; ICAR Research Team, LIRMM, University of Montpellier, CNRS, Montpellier, France.
  • Pinson L; Pathology Department, University Hospital, Normandy University, Caen, France.
  • Cavé H; Clinical Genetics Department, Montpellier University Hospital, University of Montpellier, Montpellier, France.
  • Capri Y; Obstetrical Gynecology Department, Nîmes University Hospital, University of Montpellier, Nîmes, France.
  • Faure JM; Clinical Genetics Department, Montpellier University Hospital, University of Montpellier, Montpellier, France.
  • Grosjean F; INSERM UMR_S1131, Institut de Recherche Saint-Louis, Paris University, Paris, France.
  • Sauvestre F; Genetic Department, Molecular Genetic Unit, Assistance Publique des Hôpitaux de Paris (AP-HP), Robert Debré Hospital, Paris, France.
  • Attié-Bitach T; Genetic Department, Molecular Genetic Unit, Assistance Publique des Hôpitaux de Paris (AP-HP), Robert Debré Hospital, Paris, France.
  • Pelluard F; Inserm UMR_1195, University Paris-Saclay, Saint-Aubin, France.
  • Geneviève D; Obstetrical Gynecology Department, Prenatal Diagnosis Unit, University Hospital Montpellier, University of Montpellier, Montpellier, France.
Prenat Diagn ; 42(5): 574-582, 2022 05.
Article em En | MEDLINE | ID: mdl-35278234
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Noonan Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Noonan Idioma: En Ano de publicação: 2022 Tipo de documento: Article