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HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum.
Kause, Franziska; Zhang, Rong; Ludwig, Michael; Schmiedeke, Eberhard; Rissmann, Anke; Thiele, Holger; Altmueller, Janine; Herms, Stefan; Hilger, Alina C; Hildebrandt, Friedhelm; Reutter, Heiko.
Afiliación
  • Kause F; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Zhang R; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Ludwig M; Department of Genomics, Life & Brain Center, Bonn, Germany.
  • Schmiedeke E; Department of Clinical Chemistry and Clinical Pharmacology, University of Bonn, Bonn, Germany.
  • Rissmann A; Clinic for Paediatric Surgery and Paediatric Urology, Klinikum Bremen-Mitte, Bremen, Germany.
  • Thiele H; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty, Otto-von-Guericke University, Magdeburg, Germany.
  • Altmueller J; Cologne Center for Genomics, University of Cologne, Cologne, Germany.
  • Herms S; Cologne Center for Genomics, University of Cologne, Cologne, Germany.
  • Hilger AC; Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.
  • Hildebrandt F; Department of Genomics, Life & Brain Center, Bonn, Germany.
  • Reutter H; Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.
Birth Defects Res ; 111(10): 591-597, 2019 06 01.
Article en En | MEDLINE | ID: mdl-30887706
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Canal Anal / Ano Imperforado / Radio (Anatomía) / Columna Vertebral / Tráquea / Deformidades Congénitas de las Extremidades / Proteínas HSP70 de Choque Térmico / Esófago / Cardiopatías Congénitas / Riñón Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Male Idioma: En Revista: Birth Defects Res Año: 2019 Tipo del documento: Article País de afiliación: Alemania
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Canal Anal / Ano Imperforado / Radio (Anatomía) / Columna Vertebral / Tráquea / Deformidades Congénitas de las Extremidades / Proteínas HSP70 de Choque Térmico / Esófago / Cardiopatías Congénitas / Riñón Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Male Idioma: En Revista: Birth Defects Res Año: 2019 Tipo del documento: Article País de afiliación: Alemania