Associated Papers
Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus.
Xu YJ et al.
Bmc Medical Genetics, 2011
[Frequency of 22q11 deletions in children with isolated conotruncal defects].
Shen L et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics, 2009
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