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Co-occurring non-omphalocele and non-gastroschisis anomalies among cases with congenital omphalocele and gastroschisis.
Stoll, Claude; Alembik, Yves; Roth, Marie-Paule.
Affiliation
  • Stoll C; Laboratoire de Génétique Médicale, Faculté de Médecine, University of Strasbourg, Strasbourg Cedex, France.
  • Alembik Y; Laboratoire de Génétique Médicale, Faculté de Médecine, University of Strasbourg, Strasbourg Cedex, France.
  • Roth MP; Laboratoire de Génétique Médicale, Faculté de Médecine, University of Strasbourg, Strasbourg Cedex, France.
Am J Med Genet A ; 185(7): 1954-1971, 2021 07.
Article in En | MEDLINE | ID: mdl-33881198
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Beckwith-Wiedemann Syndrome / Gastroschisis / Trisomy 18 Syndrome / Hernia, Umbilical Type of study: Diagnostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Female / Humans / Newborn Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2021 Document type: Article Affiliation country: Francia Country of publication: Estados Unidos
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Beckwith-Wiedemann Syndrome / Gastroschisis / Trisomy 18 Syndrome / Hernia, Umbilical Type of study: Diagnostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Female / Humans / Newborn Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2021 Document type: Article Affiliation country: Francia Country of publication: Estados Unidos