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DEL16P12.1P11.2

From Wikipedia, the free encyclopedia

Chromosome 16p12.2-p11.2 deletion syndrome is a gene deletion syndrome in the position 16p12.2-p11.2 of the human genome. [1]

References

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  1. ^ "Entrez Gene: Chromosome 16p12.2-p11.2 deletion syndrome". Retrieved 2014-03-12.