Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet-Reference-Cited by-同舟云学术

Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet

Published:2017-04-21 Issue:6 Volume:173 Page:1611-1619
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Lacaria Melanie¹^ORCID,Srour Myriam²³,Michaud Jacques L.⁴⁵⁶,Doja Asif⁷⁸⁹,Miller Elka¹⁰,Schwartzentruber Jeremy¹¹,Goldsmith Claire¹,Majewski Jacek¹¹,Boycott Kym M.¹⁷⁹,

Affiliation:

1. Department of Genetics; Children's Hospital of Eastern Ontario; Ottawa Ontario

2. Department of Neurology and Neurosurgery; McGill University; Montreal Quebec

3. Department of Pediatrics; McGill University; Montreal Quebec

4. Research Center; Centre Hospitalier Universitaire Sainte-Justine; Montreal Quebec

5. Department of Pediatrics; Universite de Montreal; Montreal Quebec

6. Department of Neurosciences; Universite de Montreal; Montreal Quebec

7. Children's Hospital of Eastern Ontario Research Institute; Ottawa Ontario

8. Division of Neurology; Children's Hospital of Eastern Ontario; Ottawa Ontario

9. Faculty of Medicine; University of Ottawa; Ottawa Ontario

10. Department of Medical Imaging; Children's Hospital of Eastern Ontario; Ottawa Ontario

11. Department of Human Genetics; McGill University; Montreal Quebec

Funder

Genome Quebec

Genome British Columbia

Canadian Institutes of Health Research

McLaughlin Centre

Genome Canada

Ontario Genomics Institute

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference20 articles.

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2. A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability;Cobben;European Journal of Medical Genetics,2014

3. Establishing a reference group for distal 18q-: Clinical description and molecular basis;Cody;Human Genetics,2014

4. A subterminal deletion of the long arm of chromosome 10: A clinical report and review;Courtens;American Journal of Medical Genetics Part A,2006

5. Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology;Faria;American Journal of Medical Genetics Part A,2016

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