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Dual independent genetic etiologies in a lethal complex malformation phenotype.
Filges, Isabel; Genewein, Agnes; Weber, Peter; Meier, Stephanie; Deigendesch, Nikolaus; Bruder, Elisabeth; Prüfer, Friederike; Tercanli, Sevgi.
Afiliação
  • Filges I; Medical Genetics, Institute for Medical Genetics and Pathology, University Hospital Basel and University of Basel, Switzerland.
  • Genewein A; Neonatology, University Children's Hospital Basel and University of Basel, Switzerland.
  • Weber P; Pediatric Neurology and Developmental Medicine, University Children's Hospital Basel and University of Basel, Switzerland.
  • Meier S; Medical Genetics, Institute for Medical Genetics and Pathology, University Hospital Basel and University of Basel, Switzerland.
  • Deigendesch N; Pathology, Institute for Medical Genetics and Pathology, University Hospital Basel and University of Basel, Switzerland.
  • Bruder E; Pathology, Institute for Medical Genetics and Pathology, University Hospital Basel and University of Basel, Switzerland.
  • Prüfer F; Pediatric Radiology, University Children's Hospital Basel and University of Basel, Switzerland.
  • Tercanli S; Center for Prenatal Ultrasound, Freie Strasse, Basel and University of Basel, Switzerland.
Ultraschall Med ; 41(2): 112-114, 2020 04.
Article em En | MEDLINE | ID: mdl-32259861
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Anormalidades Múltiplas Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Anormalidades Múltiplas Idioma: En Ano de publicação: 2020 Tipo de documento: Article