DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Xu Y-J, Wang J, Xu R. , et al.
Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus.
BMC Med Genet 2011;
12 (01) 169
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