The 22q11.2 deletion: From diversity to a single gene theory-Reference-Cited by-同舟云学术

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The 22q11.2 deletion: From diversity to a single gene theory

Published:2001-01 Issue:1 Volume:3 Page:2-5
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

De Decker Hendrik Paul,Lawrenson John Bernard

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference40 articles.

1. The clinical significance of 22q11 deletion;Burn;Developmental mechanisms of heart disease,1995

2. Facial appearance of patients with conotruncal anomalies;Kinouchi;Pediatrics Japan,1976

3. A study on specific peculiar facial features of conotruncal anomaly;Kinouchi;J Tokyo Wom Med Coll,1980

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1. A comprehensive list of human microdeletion and microduplication syndromes;BMC Genomic Data;2022-11-26

2. Early-onset psychosis in an adolescent with DiGeorge syndrome: A case report;South African Journal of Psychiatry;2018-02-21

3. lncRNA C22orf32-1 contributes to the tumorigenesis of nasopharyngeal carcinoma;Oncology Letters;2017-04-11

4. Del(22q11.2) Syndrome;Atlas of Genetic Diagnosis and Counseling;2017

5. predicted v. real prevalence of the 22q11.2 deletion syndrome in children with congenital heart disease presenting to Red Cross War Memorial Children’s Hospital, South Africa: A prospective study;South African Medical Journal;2016-05-25

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