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A Chinese girl with mandibular hypoplasia, deafness, progeroid features, and lipodystrophy (MDPL) diagnosed via POLD1 mutation detection
oleh: Xiu-Wen Wang, Ling-Yun Lu, Ying Xie, Xi-Jie Yu, Pei-Fang Wei
Format: | Article |
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Diterbitkan: | Wolters Kluwer 2020-08-01 |
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