Duplication 2p16 is associated with perisylvian polymicrogyria-Reference-Cited by-同舟云学术

Duplication 2p16 is associated with perisylvian polymicrogyria

Published:2019-10-29 Issue:12 Volume:179 Page:2343-2356
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Amrom Dina¹²³^ORCID,Poduri Annapurna⁴⁵,Goldman Jennifer S.⁶,Dan Bernard,Deconinck Nicolas,Pichon Bruno⁷,Nadaf Javad⁸⁹,Andermann Frederick²¹⁰¹¹,Andermann Eva¹²⁸¹⁰,Walsh Christopher A.⁵¹²¹³^ORCID,Dobyns William B.¹⁴^ORCID

Affiliation:

1. Neurogenetics Unit Montreal Neurological Institute and Hospital Montreal Quebec Canada

2. Department of Neurology & Neurosurgery McGill University Montreal Quebec Canada

3. Department of Neurology, Hôpital Universitaire des Enfants Reine Fabiola (HUDERF) Université Libre de Bruxelles (ULB) Brussels Belgium

4. Division of Epilepsy & Clinical Neurophysiology Children's Hospital Boston Massachusetts

5. Department of Neurology Children's Hospital Boston Massachusetts

6. Ludmer Centre for Neuroinformatics and Mental Health and the Department of Biomedical Engineering McGill Centre for Integrative Neuroscience, McGill University Montreal Quebec Canada

7. Department of Medical Genetics Hôpital Erasme, Université Libre de Bruxelles (ULB) Brussels Belgium

8. Department of Human Genetics McGill University Montreal Quebec Canada

9. Genome Quebec Innovation Center McGill University Montreal Quebec Canada

10. Epilepsy Research Group Montreal Neurological Institute and Hospital Montreal Quebec Canada

11. Department of Pediatrics McGill University Montreal Quebec Canada

12. Division of Genetics and Manton Center for Orphan Disease Research Children's Hospital Boston Massachusetts

13. Howard Hughes Medical Institute Harvard Medical School Boston Massachusetts

14. Department of Pediatrics (Genetics) and Neurology University of Washington, and Seattle Children's Research Institute Seattle Washington

Funder

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61342

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3. Brain malformations in a patient with deletion 2p16.1: A refinement of the phenotype to BCL11A

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