DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Kitsiou-Tzeli S, Kolialexi A, Fryssira H. , et al.
Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.
In Vivo 2004;
18 (05) 603-608
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