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Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology

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

Inoue T, Yagasaki H, Nishioka J, et al
Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology

Publication history

  • Received April 30, 2018
  • Revised August 23, 2018
  • Accepted August 24, 2018
  • First published September 21, 2018.
Online issue publication 
May 28, 2019

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