A Rare Case of 46,XX True Hermaphroditism with Hidden Mosaicism with Sex-determining Region Y Chromosome-bearing Cells in the Gonads.-Reference-Cited by-同舟云学术

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A Rare Case of 46,XX True Hermaphroditism with Hidden Mosaicism with Sex-determining Region Y Chromosome-bearing Cells in the Gonads.

Published:1998 Issue:5 Volume:37 Page:467-471
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

INDUE Hisako¹,NOMURA Masatoshi¹,YANASE Toshihiko¹,ICHINO Isao¹,GOTO Kiminobu¹,IKUYAMA Shouichiro¹,TAKAYANAGI Ryouichi¹,NAWATA Hajime¹

Affiliation:

1. The Third Department of Internal Medicine, Faculty of Medicine, Kyushu University

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

http://www.jstage.jst.go.jp/article/internalmedicine1992/37/5/37_5_467/_pdf

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification of an SRY-negative 46,XX infertility male with a heterozygous deletion downstream of SOX3 gene;Molecular Cytogenetics;2022-02-14

2. Ambiguous Genitalia;Sperling Pediatric Endocrinology;2021

3. Nonneoplastic Diseases of the Testis;Urologic Surgical Pathology;2020

4. Theoretical Postulation of the Embryological Basis of the Virgin Birth and Role of Embryonic Stem Cells Localized Out of the Embryo;Human Fetal Growth and Development;2016

5. Perspectives in Pediatric Pathology, Chapter 7. Ovotesticular DSD (True Hermaphroditism);Pediatric and Developmental Pathology;2015-09

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