Your browser doesn't support javascript.
loading
Smith-Lemli-Opitz syndrome - Fetal phenotypes with special reference to the syndrome-specific internal malformation pattern.
Schoner, Katharina; Witsch-Baumgartner, Martina; Behunova, Jana; Petrovic, Robert; Bald, Rainer; Kircher, Susanne G; Ramaswamy, Annette; Kluge, Britta; Meyer-Wittkopf, Matthias; Schmitz, Ralf; Fritz, Barbara; Zschocke, Johannes; Laccone, Franco; Rehder, Helga.
Afiliação
  • Schoner K; Institute of Pathology, Philipps-University Marburg, Marburg, Germany.
  • Witsch-Baumgartner M; Institute of Human Genetics, Medical University Innsbruck, Innsbruck, Austria.
  • Behunova J; Institute of Medical Genetics, Medical University Vienna, Vienna, Austria.
  • Petrovic R; Institute of Medical Biology, Comenius University Bratislava, Bratislava, Slovakia.
  • Bald R; Clinic of Gynecology and Obstetrics, Klinikum Leverkusen, Leverkusen, Germany.
  • Kircher SG; Institute of Medical Genetics, Medical University Vienna, Vienna, Austria.
  • Ramaswamy A; Institute of Pathology, Philipps-University Marburg, Marburg, Germany.
  • Kluge B; Institute of Medical Genetics, Medical University Vienna, Vienna, Austria.
  • Meyer-Wittkopf M; Clinic of Gynecology and Obstetrics, University Clinic Oldenburg, Oldenburg, Germany.
  • Schmitz R; Clinic of Gynecology and Obstetrics, University Clinic Muenster, Münster, Germany.
  • Fritz B; Institute of Human Genetics, Philipps-University Marburg, Marburg, Germany.
  • Zschocke J; Institute of Human Genetics, Medical University Innsbruck, Innsbruck, Austria.
  • Laccone F; Institute of Medical Genetics, Medical University Vienna, Vienna, Austria.
  • Rehder H; Institute of Pathology, Philipps-University Marburg, Marburg, Germany.
Birth Defects Res ; 112(2): 175-185, 2020 01 15.
Article em En | MEDLINE | ID: mdl-31840946
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Smith-Lemli-Opitz Tipo de estudo: Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Revista: Birth Defects Res Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Smith-Lemli-Opitz Tipo de estudo: Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Revista: Birth Defects Res Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha