Can clinical assessment detect 22q11.2 deletions in patients with cardiac malformations? A review
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference37 articles.
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2. Screening of patients at risk for 22q11 deletion;Barisic;Coll. Antropol.,2008
3. Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies;Beauchesne;J. Am. Coll. Cardiol.,2005
4. A search for chromosome 22q11.2 deletions in a series of 176 consecutively catheterized patients with congenital heart disease: no evidence for deletions in non-syndromic patients;Borgmann;Eur. J. Pediatr.,1999
5. A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population;Botto;Pediatrics,2003
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