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CDKN1C hyperexpression in two patients with severe growth failure and microdeletions affecting the paternally inherited KCNQ1OT1:TSS-DMR

Authors

  1. Correspondence to Dr Masayo Kagami, Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo 157-8535, Japan; kagami-ms{at}ncchd.go.jp
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Citation

Hara-Isono K, Yamazawa K, Tanaka S, et al
CDKN1C hyperexpression in two patients with severe growth failure and microdeletions affecting the paternally inherited KCNQ1OT1:TSS-DMR

Publication history

  • Received May 18, 2022
  • Accepted July 19, 2022
  • First published July 29, 2022.

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