Acromicric dysplasia caused by a mutation of fibrillin 1 in a family: A case report.

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第一作者： Ren,Shen

第一单位： Department of Pediatrics, The People's Hospital of Yuhuan, Taizhou 317600, Zhejiang Province, China.

作者： Ren,Shen ^[1] ; Jian-Hua,Feng ^[2] ; Shan-Pu,Yang ^[3]

作者单位： Department of Pediatrics, The People's Hospital of Yuhuan, Taizhou 317600, Zhejiang Province, China. ^[1] Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, Zhejiang Province, China. ^[2] Department of Pediatrics, The People's Hospital of Yuhuan, Taizhou 317600, Zhejiang Province, China. ysp6005@qq.com. ^[3]

关键词 Acromicric dysplasia Case report Fibrillin 1 Gene Recombinant human growth hormone Short stature

DOI 10.12998/wjcc.v11.i9.2036

PMID 36998968

发布时间 2023-04-01

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World journal of clinical cases

2023年11卷9期

2036-2042页

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Acromicric dysplasia caused by a mutation of fibrillin 1 in a family: A case report.

World journal of clinical cases

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World journal of clinical cases

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Acromicric dysplasia caused by a mutation of fibrillin 1 in a family: A case report.

World journal of clinical cases

相似文献

World journal of clinical cases

相关期刊

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