DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Iserin L, de Lonlay P, Viot G. et al.
Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies.
Eur J Pediatr 1998;
157 (11) 881-884
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