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A commentary on ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin-Siris-like

Tadashi Kaname1, Kumiko Yanagi1

  • 1Department of Genome Medicine, National Center for Child Health and Development, Tokyo, Japan.

Journal of Human Genetics
|June 2, 2017
PubMed
Abstract

No abstract available in PubMed .

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