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Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF.
Filges, Isabel; Bruder, Elisabeth; Brandal, Kristin; Meier, Stephanie; Undlien, Dag Erik; Waage, Trine Rygvold; Hoesli, Irene; Schubach, Max; de Beer, Tjaart; Sheng, Ying; Hoeller, Sylvia; Schulzke, Sven; Røsby, Oddveig; Miny, Peter; Tercanli, Sevgi; Oppedal, Truls; Meyer, Peter; Selmer, Kaja Kristine; Strømme, Petter.
Afiliação
  • Filges I; Medical Genetics, University Hospital Basel, Basel, Switzerland.
  • Bruder E; Pathology, University Hospital Basel, Basel, Switzerland.
  • Brandal K; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
  • Meier S; Medical Genetics, University Hospital Basel, Basel, Switzerland.
  • Undlien DE; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
  • Waage TR; Section of Paediatric Neurohabilitation, Department of Clinical Neurosciences for Children, Oslo University Hospital, Ullevål, Oslo, Norway.
  • Hoesli I; Obstetrics and Gynecology, University Hospital Basel, Basel, Switzerland.
  • Schubach M; Institute for Medical and Human Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • de Beer T; Biozentrum and Swiss Institute of Bioinformatics, University of Basel, Basel, Switzerland.
  • Sheng Y; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
  • Hoeller S; Pathology, University Hospital Basel, Basel, Switzerland.
  • Schulzke S; Neonatology, University Children's Hospital Basel, Basel, Switzerland.
  • Røsby O; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
  • Miny P; Medical Genetics, University Hospital Basel, Basel, Switzerland.
  • Tercanli S; Centre for Prenatal Ultrasound, Basel, Switzerland.
  • Oppedal T; Department of Ophthalmology, Section for Pediatric Ophthalmology, Oslo University Hospital, Ullevål, Oslo, Norway.
  • Meyer P; Pathology, University Hospital Basel, Basel, Switzerland.
  • Selmer KK; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
  • Strømme P; Section for Clinical Neurosciences, Department of Pediatrics, Oslo University Hospital and University of Oslo, Oslo, Norway.
Hum Mutat ; 37(7): 711, 2016 07.
Article em En | MEDLINE | ID: mdl-27300082
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Suíça
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Suíça