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De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry.

Journal: American Journal of Human Genetics

Published: 2019-10-11

DOI: 10.1016/j.ajhg.2019.09.022

Affiliations: 23

Authors: 30

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Institutions Share
Department of General Pediatrics, WWU, Germany 0.37
Division of Paediatric Respiratory Medicine, Royal Brompton Hospital, United Kingdom (UK) 0.08
Institute of Medical Informatics (IMI), WWU, Germany 0.07
UNC Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center (CF Center), United States of America (USA) 0.05
UNC Department of Pediatrics, United States of America (USA) 0.05
UCL Genetics and Genomic Medicine Programme, United Kingdom (UK) 0.03
Edward Mallinckrodt Department of Pediatrics, WUSTL, United States of America (USA) 0.03
John T. Milliken Department of Medicine, WUSTL, United States of America (USA) 0.03
University Hospital Carl Gustav Carus Dresden, TU Dresden, Germany 0.03
The Altona Children's Hospital, Germany 0.03
Department of Neurosurgery, WWU, Germany 0.03
Cologne Center for Genomics (CCG), UoC, Germany 0.03
Center for Molecular Medicine Cologne (CMMC), UoC, Germany 0.03
National Heart and Lung Institute (NHLI), ICL, United Kingdom (UK) 0.02
UNC Department of Medicine, United States of America (USA) 0.02
Royal Brompton Hospital, United Kingdom (UK) 0.02
Division of Molecular and Clinical Medicine, University of Dundee, United Kingdom (UK) 0.02
Department of Genetics, WUSTL, United States of America (USA) 0.02
UNC Department of Pathology and Laboratory Medicine, United States of America (USA) 0.02
McDonnell Genome Institute (MGI), WUSTL, United States of America (USA) 0.02

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