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MOESM1 of Cleidocranial dysplasia with growth hormone deficiency: a case report

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posted on 2020-01-17, 04:52 authored by Nozomi Takaki, Jun Mori, Satoshi Matsuo, Toshio Osamura, Toshimi Michigami
Additional file 1: Table S1. Primer sets used for the RUNX2 mutation analysis.

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