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Atypical fibrodysplasia ossificans progressiva diagnosed by whole‐exome sequencing
Authors:Hao Liu  Sarah L Sawyer  Monika Gos  David Grynspan  Kheirie Issa  Raveena Ramphal  Carmen Rotaru  FORGE Canada Consortium  Jacek Majewski  Kym M Boycott  Gail Graham  Matthew Bromwich
Affiliation:1. Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada;2. Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada;3. Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada;4. Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland;5. Department of Pathology, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada;6. Division of General Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada;7. Division of Hematology/Oncology, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada;8. Department of Diagnostic Imaging, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada;9. FORGE steering committee are listed in the acknowledgments;10. Department of Human Genetics, McGill University, Montreal, Canada;11. Division of Otolaryngology, Head and Neck Surgery, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada
Abstract:
Keywords:fibrodysplasia ossificans progressiva  heterotopic ossification  hallux valgus  whole exome sequencing
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