Your browser doesn't support javascript.
loading
Atypical fibrodysplasia ossificans progressiva diagnosed by whole-exome sequencing.
Liu, Hao; Sawyer, Sarah L; Gos, Monika; Grynspan, David; Issa, Kheirie; Ramphal, Raveena; Rotaru, Carmen; Majewski, Jacek; Boycott, Kym M; Graham, Gail; Bromwich, Matthew.
Affiliation
  • Liu H; Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
  • Sawyer SL; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.
  • Gos M; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.
  • Grynspan D; Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland.
  • Issa K; Department of Pathology, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.
  • Ramphal R; Division of General Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.
  • Rotaru C; Division of Hematology/Oncology, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.
  • Boycott KM; Department of Human Genetics, McGill University, Montreal, QC, Canada.
  • Graham G; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.
  • Bromwich M; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.
Am J Med Genet A ; 167(6): 1337-41, 2015 Jun.
Article in En | MEDLINE | ID: mdl-25899773
Subject(s)
Key words
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Distress Syndrome, Newborn / Hallux Valgus / Activin Receptors, Type I / Fetal Growth Retardation / Mutation / Myositis Ossificans Type of study: Diagnostic_studies / Prognostic_studies Limits: Child, preschool / Female / Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2015 Type: Article Affiliation country: Canada
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Distress Syndrome, Newborn / Hallux Valgus / Activin Receptors, Type I / Fetal Growth Retardation / Mutation / Myositis Ossificans Type of study: Diagnostic_studies / Prognostic_studies Limits: Child, preschool / Female / Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2015 Type: Article Affiliation country: Canada