Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patients-Reference-Cited by-同舟云学术

Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patients

Published:2019-01 Issue:1 Volume:62 Page:27-34
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Gazdagh Gabriella,Blyth Moira,Scurr Ingrid,Turnpenny Peter D.,Mehta Sarju G.^ORCID,Armstrong Ruth,McEntagart Meriel,Newbury-Ecob Ruth,Tobias Edward S.,Joss Shelagh

Funder

Health Innovation Challenge Fund

Wellcome Trust

Department of Health

Wellcome Trust Sanger Institute

Cambridge South REC

Republic of Ireland REC

National Institute for Health Research

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

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3. ARID2, a rare cause of Coffin‐Siris syndrome: A novel microdeletion at 12q12q13.11 causing severe short stature and literature review;American Journal of Medical Genetics Part A;2023-02-09

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