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Further evidence for complex inheritance of holoprosencephaly: Lessons learned from pre- and postnatal diagnostic testing in Germany.
Hinreiner, Sophie; Wieczorek, Dagmar; Mueller, Dietmar; Roedl, Tanja; Thiel, Gundula; Grasshoff, Ute; Chaoui, Rabih; Hehr, Ute.
Afiliação
  • Hinreiner S; Center for Human Genetics Regensburg, Regensburg, Germany.
  • Wieczorek D; Medical Faculty, Institute of Human Genetics, Heinrich-Heine-University Duesseldorf, Duesseldorf, Germany.
  • Mueller D; Department of Medical Genetics, Children's Hospital Chemnitz, Chemnitz, Germany.
  • Roedl T; Center for Human Genetics Regensburg, Regensburg, Germany.
  • Thiel G; Center for Prenatal Diagnosis and Human Genetics, Berlin, Germany.
  • Grasshoff U; Institute of Medical Genetics and Applied Genomics, University Hospital Tuebingen, Tuebingen, Germany.
  • Chaoui R; Center for Prenatal Diagnosis and Human Genetics, Berlin, Germany.
  • Hehr U; Center for Human Genetics Regensburg, Regensburg, Germany.
Am J Med Genet C Semin Med Genet ; 178(2): 198-205, 2018 06.
Article em En | MEDLINE | ID: mdl-30182445
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Holoprosencefalia / Mutação Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male / Pregnancy País/Região como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes Genéticos / Holoprosencefalia / Mutação Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male / Pregnancy País/Região como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article