Open AccessAB061. Prevalence of 22q11.2 deletion syndrome in patients with congenital heart diseases in North-eastern Thailand
Author(s) -
Panuwat Srichaisawat,
Khunton Wichajarn,
Arnkisa Chaikitpinyo,
Manat Panamonta,
Jureeporn Kampan
Publication year - 2017
Publication title -
annals of translational medicine
Language(s) - English
Resource type - Journals
eISSN - 2305-5847
pISSN - 2305-5839
DOI - 10.21037/atm.2017.s061
Subject(s) - medicine , deletion syndrome , pediatrics , genetics , biology , gene , phenotype
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