Clinical and Genetic Analyses of Two Unrelated 46, XX Girls with Combined 17α-Hydroxylase/17,20-lyase Deficiency from China.

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作者： Yamei,Li ^[1] ; Ting,Han ^[2] ; Yingxia,Wang ^[1] ; Jie,Gao ^[1] ; Jianglin,Zhang ^[1] ; Yinglan,Wu ^[1]

作者单位： Department of Women Health Care, Hunan Provincial Maternal and Child Health Care Hospital. ^[1] NHC Key Laboratory for Birth Defect for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital. ^[2]

关键词 17α-hydroxylase/17,20-lyase deficiency Congenital adrenal hyperplasia Cytochrome P450 Family 17 Subfamily A Member 1 gene mutation nocturnal enuresis

DOI 10.4274/jcrpe.galenos.2023.2022-8-7

PMID 36800681

发布时间 2024-02-16

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Journal of clinical research in pediatric endocrinology

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Clinical and Genetic Analyses of Two Unrelated 46, XX Girls with Combined 17α-Hydroxylase/17,20-lyase Deficiency from China.

Journal of clinical research in pediatric endocrinology

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Journal of clinical research in pediatric endocrinology

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Clinical and Genetic Analyses of Two Unrelated 46, XX Girls with Combined 17α-Hydroxylase/17,20-lyase Deficiency from China.

Journal of clinical research in pediatric endocrinology

相似文献

Journal of clinical research in pediatric endocrinology

相关期刊

检索历史清除