DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Kuo YL, Chen CP, Wang LK. , et al.
Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
Taiwan J Obstet Gynecol 2014;
53 (02) 248-251
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