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Clinical Follow-Up of a Novel NR0B1 Mutation in a Case of Adrenal Hypoplasia Congenital | ESPE2019
haihua yang; haiyan wei; Linghua Shen; Huizhen Wang; Qiong Chen; Yongxing Chen; Xiaojing Liu
http://abstracts.eurospe.org/hrp/0092/hrp0092P3-12
Published: 2019-08-22

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A Novel Missense COL10A1 Mutation Identified by Next Generation Sequencing in a Chinese Pedigree with Schmid Metaphyseal Chondrodysplasia | ESPE2019
Qiong Chen; Shengnan Wu; Yongxing Chen; Haiyan Wei
http://abstracts.eurospe.org/hrp/0092/hrp0092P2-55
Published: 2019-08-22

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Clinical Follow-Up of a Novel NR0B1 Mutation in a Case of Adrenal Hypoplasia Congenital | ESPE2019
haihua yang; haiyan wei; Linghua Shen; Huizhen Wang; Qiong Chen; Yongxing Chen; Xiaojing Liu
http://abstracts.eurospe.org/hrp/0092/hrp0092p3-12.html
Published: 2019-08-22

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A Novel Missense COL10A1 Mutation Identified by Next Generation Sequencing in a Chinese Pedigree with Schmid Metaphyseal Chondrodysplasia | ESPE2019
Qiong Chen; Shengnan Wu; Yongxing Chen; Haiyan Wei
http://abstracts.eurospe.org/hrp/0092/hrp0092p2-55.html
Published: 2019-08-22

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