An Extremely Rare <i>SRD5A2</i> Gene c.485A>C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam.

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作者： Phan Tuong Quynh,Le ^[1] ; Thanh Nha Uyen,Le ^[2] ; Thi Thanh Binh,Nguyen ^[1] ; Minh Thao,Nguyen ^[3] ; Thi Minh Thi,Ha ^[4]

作者单位： Department of Medical Genetics, University of Medicine and Pharmacy, Hue University, Hue, Vietnam. ^[1] Center of Prenatal and Neonatal Screening-Diagnosis, University of Medicine and Pharmacy Hospital, Hue University, Hue, Vietnam. ^[2] Department of Pediatrics, University of Medicine and Pharmacy, Hue University, Hue, Vietnam. ^[3] Department of Anatomy and Surgical Training, University of Medicine and Pharmacy, Hue University, Hue, Vietnam. ^[4]

DOI 10.1155/2022/6025916

PMID 35386187

发布时间 2022-04-08

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Case reports in endocrinology

2022年2022卷

6025916页

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An Extremely Rare <i>SRD5A2</i> Gene c.485A>C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam.

Case reports in endocrinology

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Case reports in endocrinology

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An Extremely Rare <i>SRD5A2</i> Gene c.485A&gt;C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam.

Case reports in endocrinology

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Case reports in endocrinology

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An Extremely Rare <i>SRD5A2</i> Gene c.485A>C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam.