Interlytiškumas (Lithuanian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Interlytiškumas" in Lithuanian language version.

refsWebsite

Global rank Lithuanian rank

24nih.gov

4^th place

12^th place

13doi.org

2^nd place

10^th place

8web.archive.org

1^st place

5semanticscholar.org

11^th place

926^th place

2worldcat.org

5^th place

16^th place

1ohchr.org

1,210^th place

3,417^th place

1unfe.org

low place

3,229^th place

1britannica.com

40^th place

8^th place

1leonardsax.com

low place

1urologyhealth.org

low place

1rarediseases.org

5,181^st place

low place

britannica.com

„Reproductive system disease - Intersexuality“. Encyclopedia Britannica. Nuoroda tikrinta 2021-07-22.

doi.org

Selma Feldman Witchel (2018). „Disorders of Sex Development“. Best Practice & Research. Clinical Obstetrics & Gynaecology. 48: 90–102. doi:10.1016/j.bpobgyn.2017.11.005. ISSN 1521-6934. PMC 5866176. PMID 29503125.
Sax, Leonard (2002 m. rugpjūčio mėn.). „How common is intersex? a response to Anne Fausto-Sterling“. Journal of Sex Research. 39 (3): 174–178. doi:10.1080/00224490209552139. ISSN 0022-4499. PMID 12476264. S2CID 33795209. Suarchyvuotas originalas 24 April 2021. Alt URL
Witchel, Selma Feldman; Azziz, Ricardo (2010). „Nonclassic Congenital Adrenal Hyperplasia“. International Journal of Pediatric Endocrinology. 2010: 625105. doi:10.1155/2010/625105. PMC 2910408. PMID 20671993.
Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, Meyer-Bahlburg HF, Miller WL, Murad MH, Oberfield SE, White PC (November 2018). „Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline“. The Journal of Clinical Endocrinology and Metabolism. 103 (11): 4043–4088. doi:10.1210/jc.2018-01865. PMC 6456929. PMID 30272171.
Springer, A.; van den Heijkant, M.; Baumann, S. (June 2016). „Worldwide prevalence of hypospadias“. Journal of Pediatric Urology. 12 (3): 152.e1–152.e7. doi:10.1016/j.jpurol.2015.12.002. PMID 26810252.
Wigby, Kristen; D'Epagnier, Cheryl; Howell, Susan; Reicks, Amy; Wilson, Rebecca; Cordeiro, Lisa; Tartaglia, Nicole (November 2016). „Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis“. American Journal of Medical Genetics Part A. 170 (11): 2870–2881. doi:10.1002/ajmg.a.37688. PMC 6501572. PMID 27644018.
Morcel, Karine; Camborieux, Laure; Guerrier, Daniel (2007). „Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome“. Orphanet Journal of Rare Diseases. 2 (1): 13. doi:10.1186/1750-1172-2-13. PMC 1832178. PMID 17359527.{{cite journal}}: CS1 priežiūra: unflagged free DOI (link)
Mohammadpour Lashkari, F.; Sadighi Gilani, M. A.; Ghaheri, A.; Zamanian, M. R.; Borjian Boroujeni, P.; Mohseni Meybodi, A.; Sabbaghian, M. (June 2018). „Clinical aspects of 49 infertile males with 45,X/46,XY mosaicism karyotype: A case series“. Andrologia. 50 (5): e13009. doi:10.1111/and.13009. PMID 29527714. S2CID 3833188. „Chromosomal analysis plays an important role in the DSD determination. 45,X/46,XY mosaicism is a rare karyotype, and its prevalence is about 1.5 in 10,000 newborns.“
Stochholm, Kirstine; Juul, Svend; Gravholt, Claus H (2010). „Diagnosis and mortality in 47,XYY persons: a registry study“. Orphanet Journal of Rare Diseases. 5 (1): 15. doi:10.1186/1750-1172-5-15. PMC 2889887. PMID 20509956.{{cite journal}}: CS1 priežiūra: unflagged free DOI (link)
Merke DP, Auchus RJ (September 2020). „Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency“. The New England Journal of Medicine. 383 (13): 1248–1261. doi:10.1056/NEJMra1909786. PMID 32966723. S2CID 221884108.
Tartaglia, Nicole; Ayari, Natalie; Howell, Susan; D'Epagnier, Cheryl; Zeitler, Philip (June 2011). „48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome“. Acta Paediatrica. 100 (6): 851–860. doi:10.1111/j.1651-2227.2011.02235.x. PMC 3314712. PMID 21342258.
Sinnecker, G. H. G.; Hiort, O.; Nitsche, E. M.; Holterhus, P.-M.; Kruse, K.; Group, German Collaborative Intersex Study (29 June 1996). „Functional assessment and clinical classification of androgen sensitivity in patients with mutations of the androgen receptor gene“. European Journal of Pediatrics. 156 (1): 7–14. doi:10.1007/s004310050542. PMID 9007482. S2CID 34427651. Suarchyvuota iš originalo 29 August 2020. Nuoroda tikrinta 5 February 2020. „In the genetic male, mutations of the androgen receptor (AR) gene cause phenotypes ranging from female to subfertile male.“
Boehmer, Annemie L. M.; Brüggenwirth, Hennie; van Assendelft, Cissy; Otten, Barto J.; Verleun-Mooijman, Marja C. T.; Niermeijer, Martinus F.; Brunner, Han G.; Rouwé, Catrienus W.; Waelkens, J. J.; Oostdijk, Wilma; Kleijer, Wim J.; van der Kwast, Theo H.; de Vroede, Monique A.; Drop, Stenvert L. S. (September 2001). „Genotype Phenotype in Families with Androgen Insensitivity Syndrome“. The Journal of Clinical Endocrinology & Metabolism. 86 (9): 4151–4160. doi:10.1210/jcem.86.9.7825. PMID 11549642.

leonardsax.com

Sax, Leonard (2002 m. rugpjūčio mėn.). „How common is intersex? a response to Anne Fausto-Sterling“. Journal of Sex Research. 39 (3): 174–178. doi:10.1080/00224490209552139. ISSN 0022-4499. PMID 12476264. S2CID 33795209. Suarchyvuotas originalas 24 April 2021. Alt URL

nih.gov

pubmed.ncbi.nlm.nih.gov

Selma Feldman Witchel (2018). „Disorders of Sex Development“. Best Practice & Research. Clinical Obstetrics & Gynaecology. 48: 90–102. doi:10.1016/j.bpobgyn.2017.11.005. ISSN 1521-6934. PMC 5866176. PMID 29503125.
Sax, Leonard (2002 m. rugpjūčio mėn.). „How common is intersex? a response to Anne Fausto-Sterling“. Journal of Sex Research. 39 (3): 174–178. doi:10.1080/00224490209552139. ISSN 0022-4499. PMID 12476264. S2CID 33795209. Suarchyvuotas originalas 24 April 2021. Alt URL
Witchel, Selma Feldman; Azziz, Ricardo (2010). „Nonclassic Congenital Adrenal Hyperplasia“. International Journal of Pediatric Endocrinology. 2010: 625105. doi:10.1155/2010/625105. PMC 2910408. PMID 20671993.
Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, Meyer-Bahlburg HF, Miller WL, Murad MH, Oberfield SE, White PC (November 2018). „Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline“. The Journal of Clinical Endocrinology and Metabolism. 103 (11): 4043–4088. doi:10.1210/jc.2018-01865. PMC 6456929. PMID 30272171.
Springer, A.; van den Heijkant, M.; Baumann, S. (June 2016). „Worldwide prevalence of hypospadias“. Journal of Pediatric Urology. 12 (3): 152.e1–152.e7. doi:10.1016/j.jpurol.2015.12.002. PMID 26810252.
Wigby, Kristen; D'Epagnier, Cheryl; Howell, Susan; Reicks, Amy; Wilson, Rebecca; Cordeiro, Lisa; Tartaglia, Nicole (November 2016). „Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis“. American Journal of Medical Genetics Part A. 170 (11): 2870–2881. doi:10.1002/ajmg.a.37688. PMC 6501572. PMID 27644018.
Morcel, Karine; Camborieux, Laure; Guerrier, Daniel (2007). „Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome“. Orphanet Journal of Rare Diseases. 2 (1): 13. doi:10.1186/1750-1172-2-13. PMC 1832178. PMID 17359527.{{cite journal}}: CS1 priežiūra: unflagged free DOI (link)
Mohammadpour Lashkari, F.; Sadighi Gilani, M. A.; Ghaheri, A.; Zamanian, M. R.; Borjian Boroujeni, P.; Mohseni Meybodi, A.; Sabbaghian, M. (June 2018). „Clinical aspects of 49 infertile males with 45,X/46,XY mosaicism karyotype: A case series“. Andrologia. 50 (5): e13009. doi:10.1111/and.13009. PMID 29527714. S2CID 3833188. „Chromosomal analysis plays an important role in the DSD determination. 45,X/46,XY mosaicism is a rare karyotype, and its prevalence is about 1.5 in 10,000 newborns.“
Stochholm, Kirstine; Juul, Svend; Gravholt, Claus H (2010). „Diagnosis and mortality in 47,XYY persons: a registry study“. Orphanet Journal of Rare Diseases. 5 (1): 15. doi:10.1186/1750-1172-5-15. PMC 2889887. PMID 20509956.{{cite journal}}: CS1 priežiūra: unflagged free DOI (link)
Merke DP, Auchus RJ (September 2020). „Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency“. The New England Journal of Medicine. 383 (13): 1248–1261. doi:10.1056/NEJMra1909786. PMID 32966723. S2CID 221884108.
Tartaglia, Nicole; Ayari, Natalie; Howell, Susan; D'Epagnier, Cheryl; Zeitler, Philip (June 2011). „48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome“. Acta Paediatrica. 100 (6): 851–860. doi:10.1111/j.1651-2227.2011.02235.x. PMC 3314712. PMID 21342258.
Sinnecker, G. H. G.; Hiort, O.; Nitsche, E. M.; Holterhus, P.-M.; Kruse, K.; Group, German Collaborative Intersex Study (29 June 1996). „Functional assessment and clinical classification of androgen sensitivity in patients with mutations of the androgen receptor gene“. European Journal of Pediatrics. 156 (1): 7–14. doi:10.1007/s004310050542. PMID 9007482. S2CID 34427651. Suarchyvuota iš originalo 29 August 2020. Nuoroda tikrinta 5 February 2020. „In the genetic male, mutations of the androgen receptor (AR) gene cause phenotypes ranging from female to subfertile male.“
Boehmer, Annemie L. M.; Brüggenwirth, Hennie; van Assendelft, Cissy; Otten, Barto J.; Verleun-Mooijman, Marja C. T.; Niermeijer, Martinus F.; Brunner, Han G.; Rouwé, Catrienus W.; Waelkens, J. J.; Oostdijk, Wilma; Kleijer, Wim J.; van der Kwast, Theo H.; de Vroede, Monique A.; Drop, Stenvert L. S. (September 2001). „Genotype Phenotype in Families with Androgen Insensitivity Syndrome“. The Journal of Clinical Endocrinology & Metabolism. 86 (9): 4151–4160. doi:10.1210/jcem.86.9.7825. PMID 11549642.

ncbi.nlm.nih.gov

Selma Feldman Witchel (2018). „Disorders of Sex Development“. Best Practice & Research. Clinical Obstetrics & Gynaecology. 48: 90–102. doi:10.1016/j.bpobgyn.2017.11.005. ISSN 1521-6934. PMC 5866176. PMID 29503125.
Witchel, Selma Feldman; Azziz, Ricardo (2010). „Nonclassic Congenital Adrenal Hyperplasia“. International Journal of Pediatric Endocrinology. 2010: 625105. doi:10.1155/2010/625105. PMC 2910408. PMID 20671993.
Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, Meyer-Bahlburg HF, Miller WL, Murad MH, Oberfield SE, White PC (November 2018). „Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline“. The Journal of Clinical Endocrinology and Metabolism. 103 (11): 4043–4088. doi:10.1210/jc.2018-01865. PMC 6456929. PMID 30272171.
Wigby, Kristen; D'Epagnier, Cheryl; Howell, Susan; Reicks, Amy; Wilson, Rebecca; Cordeiro, Lisa; Tartaglia, Nicole (November 2016). „Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis“. American Journal of Medical Genetics Part A. 170 (11): 2870–2881. doi:10.1002/ajmg.a.37688. PMC 6501572. PMID 27644018.
Morcel, Karine; Camborieux, Laure; Guerrier, Daniel (2007). „Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome“. Orphanet Journal of Rare Diseases. 2 (1): 13. doi:10.1186/1750-1172-2-13. PMC 1832178. PMID 17359527.{{cite journal}}: CS1 priežiūra: unflagged free DOI (link)
Stochholm, Kirstine; Juul, Svend; Gravholt, Claus H (2010). „Diagnosis and mortality in 47,XYY persons: a registry study“. Orphanet Journal of Rare Diseases. 5 (1): 15. doi:10.1186/1750-1172-5-15. PMC 2889887. PMID 20509956.{{cite journal}}: CS1 priežiūra: unflagged free DOI (link)
Tartaglia, Nicole; Ayari, Natalie; Howell, Susan; D'Epagnier, Cheryl; Zeitler, Philip (June 2011). „48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome“. Acta Paediatrica. 100 (6): 851–860. doi:10.1111/j.1651-2227.2011.02235.x. PMC 3314712. PMID 21342258.

ghr.nlm.nih.gov

Reference, Genetics Home. „Turner syndrome“. Genetics Home Reference. Suarchyvuota iš originalo 29 August 2020. Nuoroda tikrinta 19 December 2019.
„46,XX testicular disorder of sex development“. Genetics Home Reference. Suarchyvuota iš originalo 17 May 2019. Nuoroda tikrinta 24 December 2019.
Reference, Genetics Home. „Swyer syndrome“. Genetics Home Reference. Suarchyvuotas originalas 16 December 2019. Nuoroda tikrinta 21 December 2019.

rarediseases.info.nih.gov

„Klinefelter syndrome Genetic and Rare Diseases Information Center (GARD) – an NCATS Program“. rarediseases.info.nih.gov. Suarchyvuota iš originalo 29 August 2020. Nuoroda tikrinta 19 December 2019.

ohchr.org

JTO komitetas prieš smurtą; JTO vaiko teisių komitetas; JTO neįgalių žmonių tiesių komitetas; JTO kankinimų ir kitokio žiauraus, nežmogiško, žeminančio elgesio ir bausmių prevencijos komitetas; Juan Méndez, specialusis pranešėjas kankinimo ir kitokio žiauraus nežmoniško ar žeminančio elgesio ar bausmės klausimais; Dainius Pῡras, specialusis pranešėjas dėl kiekvieno teisės į aukščiausią įmanomą fizinės ir psichinės sveikatos lygį; Dubravka Šimonoviæ, specialioji pranešėja smurto prieš moteris, jo priežasčių ir pasekmių klausimais; Marta Santos Pais, JT Generalinio Sekretoriaus specialioji įgaliotinė smurto prieš vaikus klausimais; Afrikos žmogaus ir tautų teisių komisija; Europos Tarybos žmogaus teisių komisaras; Amerikos žmogaus teisių komisija (2016-10-24), „Intersex Awareness Day – Wednesday 26 October. End violence and harmful medical practices on intersex children and adults, UN and regional experts urge“, Vyriausiojo žmogaus teisių komisaro biuras.

rarediseases.org

„Ovotesticular Disorder of Sex Development“. NORD (National Organization for Rare Disorders). Suarchyvuota iš originalo 29 August 2020. Nuoroda tikrinta 21 December 2019.

semanticscholar.org

api.semanticscholar.org

Sax, Leonard (2002 m. rugpjūčio mėn.). „How common is intersex? a response to Anne Fausto-Sterling“. Journal of Sex Research. 39 (3): 174–178. doi:10.1080/00224490209552139. ISSN 0022-4499. PMID 12476264. S2CID 33795209. Suarchyvuotas originalas 24 April 2021. Alt URL
Mohammadpour Lashkari, F.; Sadighi Gilani, M. A.; Ghaheri, A.; Zamanian, M. R.; Borjian Boroujeni, P.; Mohseni Meybodi, A.; Sabbaghian, M. (June 2018). „Clinical aspects of 49 infertile males with 45,X/46,XY mosaicism karyotype: A case series“. Andrologia. 50 (5): e13009. doi:10.1111/and.13009. PMID 29527714. S2CID 3833188. „Chromosomal analysis plays an important role in the DSD determination. 45,X/46,XY mosaicism is a rare karyotype, and its prevalence is about 1.5 in 10,000 newborns.“
Merke DP, Auchus RJ (September 2020). „Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency“. The New England Journal of Medicine. 383 (13): 1248–1261. doi:10.1056/NEJMra1909786. PMID 32966723. S2CID 221884108.
Sinnecker, G. H. G.; Hiort, O.; Nitsche, E. M.; Holterhus, P.-M.; Kruse, K.; Group, German Collaborative Intersex Study (29 June 1996). „Functional assessment and clinical classification of androgen sensitivity in patients with mutations of the androgen receptor gene“. European Journal of Pediatrics. 156 (1): 7–14. doi:10.1007/s004310050542. PMID 9007482. S2CID 34427651. Suarchyvuota iš originalo 29 August 2020. Nuoroda tikrinta 5 February 2020. „In the genetic male, mutations of the androgen receptor (AR) gene cause phenotypes ranging from female to subfertile male.“

semanticscholar.org

Sinnecker, G. H. G.; Hiort, O.; Nitsche, E. M.; Holterhus, P.-M.; Kruse, K.; Group, German Collaborative Intersex Study (29 June 1996). „Functional assessment and clinical classification of androgen sensitivity in patients with mutations of the androgen receptor gene“. European Journal of Pediatrics. 156 (1): 7–14. doi:10.1007/s004310050542. PMID 9007482. S2CID 34427651. Suarchyvuota iš originalo 29 August 2020. Nuoroda tikrinta 5 February 2020. „In the genetic male, mutations of the androgen receptor (AR) gene cause phenotypes ranging from female to subfertile male.“

unfe.org

„Free & Equal Campaign Fact Sheet: Intersex“ (PDF). Jungtinių Tautų vyriausiojo žmogaus teisių komisaro biuras. 2015. Originalas archyvuotas 2016-03-04. Nuoroda tikrinta 2016-03-28.

urologyhealth.org

„Urology Care Foundation – What is Vaginal Agenesis?“. www.urologyhealth.org. Suarchyvuota iš originalo 4 January 2019. Nuoroda tikrinta 2018-01-21.

web.archive.org

Sax, Leonard (2002 m. rugpjūčio mėn.). „How common is intersex? a response to Anne Fausto-Sterling“. Journal of Sex Research. 39 (3): 174–178. doi:10.1080/00224490209552139. ISSN 0022-4499. PMID 12476264. S2CID 33795209. Suarchyvuotas originalas 24 April 2021. Alt URL
„Klinefelter syndrome Genetic and Rare Diseases Information Center (GARD) – an NCATS Program“. rarediseases.info.nih.gov. Suarchyvuota iš originalo 29 August 2020. Nuoroda tikrinta 19 December 2019.
Reference, Genetics Home. „Turner syndrome“. Genetics Home Reference. Suarchyvuota iš originalo 29 August 2020. Nuoroda tikrinta 19 December 2019.
„Urology Care Foundation – What is Vaginal Agenesis?“. www.urologyhealth.org. Suarchyvuota iš originalo 4 January 2019. Nuoroda tikrinta 2018-01-21.
„46,XX testicular disorder of sex development“. Genetics Home Reference. Suarchyvuota iš originalo 17 May 2019. Nuoroda tikrinta 24 December 2019.
„Ovotesticular Disorder of Sex Development“. NORD (National Organization for Rare Disorders). Suarchyvuota iš originalo 29 August 2020. Nuoroda tikrinta 21 December 2019.
Reference, Genetics Home. „Swyer syndrome“. Genetics Home Reference. Suarchyvuotas originalas 16 December 2019. Nuoroda tikrinta 21 December 2019.
Sinnecker, G. H. G.; Hiort, O.; Nitsche, E. M.; Holterhus, P.-M.; Kruse, K.; Group, German Collaborative Intersex Study (29 June 1996). „Functional assessment and clinical classification of androgen sensitivity in patients with mutations of the androgen receptor gene“. European Journal of Pediatrics. 156 (1): 7–14. doi:10.1007/s004310050542. PMID 9007482. S2CID 34427651. Suarchyvuota iš originalo 29 August 2020. Nuoroda tikrinta 5 February 2020. „In the genetic male, mutations of the androgen receptor (AR) gene cause phenotypes ranging from female to subfertile male.“

worldcat.org

Selma Feldman Witchel (2018). „Disorders of Sex Development“. Best Practice & Research. Clinical Obstetrics & Gynaecology. 48: 90–102. doi:10.1016/j.bpobgyn.2017.11.005. ISSN 1521-6934. PMC 5866176. PMID 29503125.
Sax, Leonard (2002 m. rugpjūčio mėn.). „How common is intersex? a response to Anne Fausto-Sterling“. Journal of Sex Research. 39 (3): 174–178. doi:10.1080/00224490209552139. ISSN 0022-4499. PMID 12476264. S2CID 33795209. Suarchyvuotas originalas 24 April 2021. Alt URL