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A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndrome.
Zarrei, Mehdi; Merico, Daniele; Kellam, Barbara; Engchuan, Worrawat; Scriver, Tara; Jokhan, Rikash; Wilson, Michael D; Parr, Jeremy; Lemire, Edmond G; Stavropoulos, Dimitri J; Scherer, Stephen W.
Affiliation
  • Zarrei M; The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Merico D; Deep Genomics Inc., Toronto, Ontario, Canada.
  • Kellam B; The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Engchuan W; The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Scriver T; Royal University Hospital, Saskatoon, Saskatchewan, Canada.
  • Jokhan R; Yorkton Regional Health Center, Yorkton, Saskatchewan, Canada.
  • Wilson MD; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Parr J; Department of Molecular Genetics and McLaughlin Centre, University of Toronto, Toronto, Ontario, Canada.
  • Lemire EG; Institute of Neuroscience, Newcastle University, Newcastle Upon Tyne, UK.
  • Stavropoulos DJ; Department of Pediatrics, Royal University Hospital, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
  • Scherer SW; Department of Pediatric Laboratory Medicine, Cytogenetics Laboratory, The Hospital for Sick Children, Toronto, Ontario, Canada.
Am J Med Genet A ; 173(5): 1287-1293, 2017 May.
Article in En | MEDLINE | ID: mdl-28371330
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 4 / Cerebral Palsy / Language Development Disorders / Intellectual Disability Type of study: Prognostic_studies Limits: Adolescent / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2017 Document type: Article Affiliation country: Canada
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 4 / Cerebral Palsy / Language Development Disorders / Intellectual Disability Type of study: Prognostic_studies Limits: Adolescent / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2017 Document type: Article Affiliation country: Canada