Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome

Published:2018-03-25 Issue:4 Volume:176 Page:936-944
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Palmer Lisa D.¹,Butcher Nancy J.²³,Boot Erik¹⁴⁵,Hodgkinson Kathleen A.⁶,Heung Tracy²,Chow Eva W. C.²⁴,Guna Alina²,Crowley T. Blaine³,Zackai Elaine³⁷⁸,McDonald‐McGinn Donna M.³⁷⁸⁹,Bassett Anne S.¹²⁴⁵¹⁰^ORCID

Affiliation:

1. The Dalglish Family 22q Clinic for Adults with 22q11.2 Deletion SyndromeUniversity Health NetworkToronto Ontario Canada

2. Clinical Genetics Research ProgramCentre for Addiction and Mental HealthToronto Ontario Canada

3. The 22q and You CenterThe Children's Hospital of PhiladelphiaPhiladelphia Pennsylvania USA

4. Department of PsychiatryUniversity of TorontoToronto Ontario Canada

5. Department of PsychiatryUniversity Health NetworkToronto Ontario Canada

6. Unit of Clinical EpidemiologyMemorial University of Newfoundland, St. John's, Newfoundland Canada

7. Clinical Genetics CenterThe Children's Hospital of PhiladelphiaPhiladelphia Pennsylvania USA

8. Department of PediatricsThe Perelman School of Medicine, University of PennsylvaniaPhiladelphia Pennsylvania USA

9. Section of Genetic CounselingThe Children's Hospital of PhiladelphiaPhiladelphia Pennsylvania USA

10. Division of Cardiology, Department of Medicineand Toronto General Research Institute, University Health NetworkToronto Ontario Canada

Funder

Canadian Institutes of Health Research

National Institute of Mental Health

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.38645

Reference43 articles.

1. Patient and Family Experiences and Opinions on Adding 22q11 Deletion Syndrome to the Newborn Screen

2. Catechol-O-methyl Transferase and Expression of Schizophrenia in 73 Adults with 22q11 Deletion Syndrome

3. Premature death in adults with 22q11.2 deletion syndrome

4. Clinical features of 78 adults with 22q11 deletion syndrome

5. Neuropsychiatric aspects of 22q11.2 deletion syndrome: considerations in the prenatal setting

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