Article
Variation in prevalence of chromosome 22q11 deletion in subtypes of conotruncal defect in 254 children.
Acta paediatrica (Oslo, Norway : 1992) - 1 Sept 2011
Anilkumar A, Kappanayil M, Thampi M V, Nampoothiri S, Sundaram K R, Vasudevan D M
Abstract excerpt
AIM: To determine the frequency of chromosomal aberrations particularly 22q11 deletion in Indian children ≤2 years with different types of conotruncal malformations and their association with abnormal aortic arch. Additionally, extracardiac features were also studied. METHODS: Conventional cytogenetic and fluorescence in situ hybridization analyses were performed in 254 patients with conotruncal defects....
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