性腺形成不全 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "性腺形成不全" in Japanese language version.

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24nih.gov

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18doi.org

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1thefreedictionary.com

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1bmj.com

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1healthit.gov

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1aisia.org

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1berkeley.edu

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aisia.org

“Progress and Politics in the intersex rights movement, Feminist theory in action”. 2024年5月25日閲覧。

berkeley.edu

news.berkeley.edu

“Pesticide atrazine can turn male frogs into females”. Berkeley News, University of California. (2010).

bmj.com

jmg.bmj.com

Kusz, Kamila; Kotecki, Maciej; Wojda, Alina; Szarras-Czapnik, Maria; Latos-Bielenska, Anna; Warenik-Szymankiewicz, Alina; Ruszczynska-Wolska, Anna; Jaruzelska, Jadwiga (1 June 1999). “Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome”. Journal of Medical Genetics 36 (6): 452–456. doi:10.1136/jmg.36.6.452. PMC 1734388. PMID 10874632. https://jmg.bmj.com/content/36/6/452.

doi.org

“Andrology: Male Reproductive Health and Dysfunction”. Andrologie 11 (2): 95–97. (2001). doi:10.1007/BF03034401.
“The Testes: Disorders of Sexual Differentiation and Puberty in the Male”. Pediatric Endocrinology. 135. Elsevier Health Sciences. (2008). 662–685. doi:10.1016/B978-1-4160-4090-3.X5001-7. ISBN 9781416040903. PMC 1491552
“Pathogenesis and Treatment of Disorders of Sexual Development”. Endocrine Surgery in Children. Springer. (2018). pp. 241–270. doi:10.1007/978-3-662-54256-9_18. ISBN 978-3-662-54254-5
“Development and Pathology of the Gonad”. Seminars in Cell & Developmental Biology 45: 57–58. (2015). doi:10.1016/j.semcdb.2015.11.009. PMID 26653403.
“Pathogenesis of germ cell neoplasia in testicular dysgenesis and disorders of sex development”. Seminars in Cell & Developmental Biology 45: 124–137. (2015). doi:10.1016/j.semcdb.2015.09.013. PMID 26410164.
“46, XX Gonadal Dysgenesis With Epibulbar Dermoid”. American Journal of Medical Genetics 40 (1): 4075–4076. (1991). doi:10.1002/ajmg.1320400114. PMID 1909490.
“Disorders at the Testicular Level”. Andrology. Springer. (2010). pp. 193–238. doi:10.1007/978-3-540-78355-8_13. ISBN 978-3-540-78355-8
“46, XY disorder of sex development due to 17-beta hydroxysteroid dehydrogenase type 3 deficiency: a plea for timely genetic testing”. International Journal of Pediatric Endocrinology 12: 12. (2016). doi:10.1186/s13633-016-0030-x. PMC 4908721. PMID 27307783.
“Mutations in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure”. Cell 82 (6): 959–968. (1995). doi:10.1016/0092-8674(95)90275-9. PMID 7553856.
“Pure XY gonadal dysgenesis and agenesis in monozygotic twins”. Fertility and Sterility 85 (4): 1059.9–1059.11. (2006). doi:10.1016/j.fertnstert.2005.09.054. PMID 16580399.
“Identification of novel candidate genes for 46, XY disorders of sex development (DSD) using a C57BL/6J-Y POS mouse model”. Biology of Sex Differences 9 (8): 8. (2018). doi:10.1186/s13293-018-0167-9. PMC 5789682. PMID 29378665.
“Dysgerminoma in a case of 46, XY pure gonadal dysgenesis (Swyer Syndrome): a case report”. Diagnostic Pathology 6 (84): 84. (2011). doi:10.1186/1746-1596-6-84. PMC 3182960. PMID 21929773.
Kusz, Kamila; Kotecki, Maciej; Wojda, Alina; Szarras-Czapnik, Maria; Latos-Bielenska, Anna; Warenik-Szymankiewicz, Alina; Ruszczynska-Wolska, Anna; Jaruzelska, Jadwiga (1 June 1999). “Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome”. Journal of Medical Genetics 36 (6): 452–456. doi:10.1136/jmg.36.6.452. PMC 1734388. PMID 10874632. https://jmg.bmj.com/content/36/6/452.
“The Battle of the Sexes: Human Sex Development and Its Disorders”. Molecular Mechanisms of Cell Differentiation in Gonad Development. Results and Problems in Cell Differentiation. 58. (2006). pp. 337–382. doi:10.1007/978-3-319-31973-5_13. ISBN 978-3-319-31971-1. PMID 27300185
“Human sex-determination and disorders of sex-development (DSD)”. Seminars in Cell & Developmental Biology 45: 77–83. (2015). doi:10.1016/j.semcdb.2015.10.030. PMID 26526145.
“Mixed Gonadal Dysgenesis, Pathogenesis and Management”. Journal of Pediatric Surgery 14 (3): 287–300. (1979). doi:10.1016/s0022-3468(79)80486-8. PMID 480090.
“Turners Syndrome in adulthood”. Endocrine Reviews 23 (1): 120–140. (2002). doi:10.1210/edrv.23.1.0457. PMID 11844747.
“Turners Syndrome in adulthood”. Endocrine Reviews 23 (1): 120–140. (2002). doi:10.1210/edrv.23.1.0457. PMID 11844747.

healthit.gov

“Variation in Sex Characteristics”. www.healthit.gov. 2024年5月25日閲覧。

nih.gov

pubmed.ncbi.nlm.nih.gov

“Development and Pathology of the Gonad”. Seminars in Cell & Developmental Biology 45: 57–58. (2015). doi:10.1016/j.semcdb.2015.11.009. PMID 26653403.
“Pathogenesis of germ cell neoplasia in testicular dysgenesis and disorders of sex development”. Seminars in Cell & Developmental Biology 45: 124–137. (2015). doi:10.1016/j.semcdb.2015.09.013. PMID 26410164.
“46, XX Gonadal Dysgenesis With Epibulbar Dermoid”. American Journal of Medical Genetics 40 (1): 4075–4076. (1991). doi:10.1002/ajmg.1320400114. PMID 1909490.
“46, XY disorder of sex development due to 17-beta hydroxysteroid dehydrogenase type 3 deficiency: a plea for timely genetic testing”. International Journal of Pediatric Endocrinology 12: 12. (2016). doi:10.1186/s13633-016-0030-x. PMC 4908721. PMID 27307783.
“Mutations in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure”. Cell 82 (6): 959–968. (1995). doi:10.1016/0092-8674(95)90275-9. PMID 7553856.
“Pure XY gonadal dysgenesis and agenesis in monozygotic twins”. Fertility and Sterility 85 (4): 1059.9–1059.11. (2006). doi:10.1016/j.fertnstert.2005.09.054. PMID 16580399.
“Identification of novel candidate genes for 46, XY disorders of sex development (DSD) using a C57BL/6J-Y POS mouse model”. Biology of Sex Differences 9 (8): 8. (2018). doi:10.1186/s13293-018-0167-9. PMC 5789682. PMID 29378665.
“Dysgerminoma in a case of 46, XY pure gonadal dysgenesis (Swyer Syndrome): a case report”. Diagnostic Pathology 6 (84): 84. (2011). doi:10.1186/1746-1596-6-84. PMC 3182960. PMID 21929773.
Kusz, Kamila; Kotecki, Maciej; Wojda, Alina; Szarras-Czapnik, Maria; Latos-Bielenska, Anna; Warenik-Szymankiewicz, Alina; Ruszczynska-Wolska, Anna; Jaruzelska, Jadwiga (1 June 1999). “Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome”. Journal of Medical Genetics 36 (6): 452–456. doi:10.1136/jmg.36.6.452. PMC 1734388. PMID 10874632. https://jmg.bmj.com/content/36/6/452.
“The Battle of the Sexes: Human Sex Development and Its Disorders”. Molecular Mechanisms of Cell Differentiation in Gonad Development. Results and Problems in Cell Differentiation. 58. (2006). pp. 337–382. doi:10.1007/978-3-319-31973-5_13. ISBN 978-3-319-31971-1. PMID 27300185
“Human sex-determination and disorders of sex-development (DSD)”. Seminars in Cell & Developmental Biology 45: 77–83. (2015). doi:10.1016/j.semcdb.2015.10.030. PMID 26526145.
“Mixed Gonadal Dysgenesis, Pathogenesis and Management”. Journal of Pediatric Surgery 14 (3): 287–300. (1979). doi:10.1016/s0022-3468(79)80486-8. PMID 480090.
“Turners Syndrome in adulthood”. Endocrine Reviews 23 (1): 120–140. (2002). doi:10.1210/edrv.23.1.0457. PMID 11844747.
“Turners Syndrome in adulthood”. Endocrine Reviews 23 (1): 120–140. (2002). doi:10.1210/edrv.23.1.0457. PMID 11844747.

pmc.ncbi.nlm.nih.gov

“The Testes: Disorders of Sexual Differentiation and Puberty in the Male”. Pediatric Endocrinology. 135. Elsevier Health Sciences. (2008). 662–685. doi:10.1016/B978-1-4160-4090-3.X5001-7. ISBN 9781416040903. PMC 1491552
“46, XY disorder of sex development due to 17-beta hydroxysteroid dehydrogenase type 3 deficiency: a plea for timely genetic testing”. International Journal of Pediatric Endocrinology 12: 12. (2016). doi:10.1186/s13633-016-0030-x. PMC 4908721. PMID 27307783.
“Identification of novel candidate genes for 46, XY disorders of sex development (DSD) using a C57BL/6J-Y POS mouse model”. Biology of Sex Differences 9 (8): 8. (2018). doi:10.1186/s13293-018-0167-9. PMC 5789682. PMID 29378665.
“Dysgerminoma in a case of 46, XY pure gonadal dysgenesis (Swyer Syndrome): a case report”. Diagnostic Pathology 6 (84): 84. (2011). doi:10.1186/1746-1596-6-84. PMC 3182960. PMID 21929773.
Kusz, Kamila; Kotecki, Maciej; Wojda, Alina; Szarras-Czapnik, Maria; Latos-Bielenska, Anna; Warenik-Szymankiewicz, Alina; Ruszczynska-Wolska, Anna; Jaruzelska, Jadwiga (1 June 1999). “Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome”. Journal of Medical Genetics 36 (6): 452–456. doi:10.1136/jmg.36.6.452. PMC 1734388. PMID 10874632. https://jmg.bmj.com/content/36/6/452.

ncbi.nlm.nih.gov

nichd.nih.gov

“Turner Syndrome: Condition Information”. Eunice Kennedy Shriver National Institute of Health and Human Development (2012年). 2024年5月25日閲覧。

niehs.nih.gov

“Endocrine Disruptors, National Institute of Environmental Health Sciences, 2013”. 2024年5月25日閲覧。

thefreedictionary.com

medical-dictionary.thefreedictionary.com

“Gonadal Streak. Farlex Partner Medical Dictionary.”. 2024年5月25日閲覧。