Biology:DEL16P12.1P11.2

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Short description: Genetic element in humans

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

  1. ↑ "Entrez Gene: Chromosome 16p12.2-p11.2 deletion syndrome". https://www.ncbi.nlm.nih.gov/gene/100526742. Retrieved 2014-03-12. 




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