Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF.
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Filges I
Medical Genetics, University Hospital Basel, Basel, Switzerland.
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Bruder E
Pathology, University Hospital Basel, Basel, Switzerland.
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Brandal K
Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
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Meier S
Medical Genetics, University Hospital Basel, Basel, Switzerland.
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Undlien DE
Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
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Waage TR
Section of Paediatric Neurohabilitation, Department of Clinical Neurosciences for Children, Oslo University Hospital, Ullevål, Oslo, Norway.
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Hoesli I
Obstetrics and Gynecology, University Hospital Basel, Basel, Switzerland.
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Schubach M
Institute for Medical and Human Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany.
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de Beer T
Biozentrum and Swiss Institute of Bioinformatics, University of Basel, Basel, Switzerland.
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Sheng Y
Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
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Hoeller S
Pathology, University Hospital Basel, Basel, Switzerland.
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Schulzke S
Neonatology, University Children's Hospital Basel, Basel, Switzerland.
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Røsby O
Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
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Miny P
Medical Genetics, University Hospital Basel, Basel, Switzerland.
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Tercanli S
Centre for Prenatal Ultrasound, Basel, Switzerland.
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Oppedal T
Department of Ophthalmology, Section for Pediatric Ophthalmology, Oslo University Hospital, Ullevål, Oslo, Norway.
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Meyer P
Pathology, University Hospital Basel, Basel, Switzerland.
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Selmer KK
Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
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Strømme P
Section for Clinical Neurosciences, Department of Pediatrics, Oslo University Hospital and University of Oslo, Oslo, Norway.
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bronze
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https://folia.unifr.ch/global/documents/109739
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