References analysis of the Wikipedia article "Синдром Морріса" in the Ukrainian version

doi.org

Hughes IA, Deeb A (December 2006). Androgen resistance. Best Pract. Res. Clin. Endocrinol. Metab. 20 (4): 577—98. doi:10.1016/j.beem.2006.11.003. PMID 17161333. Galani A, Kitsiou-Tzeli S, Sofokleous C, Kanavakis E, Kalpini-Mavrou A (2008). Androgen insensitivity syndrome: clinical features and molecular defects. Hormones (Athens). 7 (3): 217—29. doi:10.14310/horm.2002.1201. PMID 18694860. Quigley CA, De Bellis A, Marschke KB, el-Awady MK, Wilson EM, French FS (June 1995). Androgen receptor defects: historical, clinical, and molecular perspectives. Endocr. Rev. 16 (3): 271—321. doi:10.1210/edrv-16-3-271. PMID 7671849.

Hughes IA, Deeb A (December 2006). Androgen resistance. Best Pract. Res. Clin. Endocrinol. Metab. 20 (4): 577—98. doi:10.1016/j.beem.2006.11.003. PMID 17161333.

Quigley CA, De Bellis A, Marschke KB, el-Awady MK, Wilson EM, French FS (June 1995). Androgen receptor defects: historical, clinical, and molecular perspectives. Endocr. Rev. 16 (3): 271—321. doi:10.1210/edrv-16-3-271. PMID 7671849.

Galani A, Kitsiou-Tzeli S, Sofokleous C, Kanavakis E, Kalpini-Mavrou A (2008). Androgen insensitivity syndrome: clinical features and molecular defects. Hormones (Athens). 7 (3): 217—29. doi:10.14310/horm.2002.1201. PMID 18694860.

Gottlieb B, Lombroso R, Beitel LK, Trifiro MA (January 2005). Molecular pathology of the androgen receptor in male (in)fertility. Reprod. Biomed. Online. 10 (1): 42—8. doi:10.1016/S1472-6483(10)60802-4. PMID 15705293.

Gottlieb B, Beitel LK, Trifiro MA (May 2001). Variable expressivity and mutation databases: The androgen receptor gene mutations database. Hum. Mutat. 17 (5): 382—8. doi:10.1002/humu.1113. PMID 11317353. S2CID 2933566.

Ozülker T, Ozpaçaci T, Ozülker F, Ozekici U, Bilgiç R, Mert M (January 2010). Incidental detection of Sertoli-Leydig cell tumor by FDG PET/CT imaging in a patient with androgen insensitivity syndrome. Ann Nucl Med. 24 (1): 35—9. doi:10.1007/s12149-009-0321-x. PMID 19957213. S2CID 10450803.

Köhler B, Lumbroso S, Leger J, Audran F, Grau ES, Kurtz F, Pinto G, Salerno M, Semitcheva T, Czernichow P, Sultan C (January 2005). Androgen insensitivity syndrome: somatic mosaicism of the androgen receptor in seven families and consequences for sex assignment and genetic counseling. J. Clin. Endocrinol. Metab. 90 (1): 106—11. doi:10.1210/jc.2004-0462. PMID 15522944.

Hiort O, Sinnecker GH, Holterhus PM, Nitsche EM, Kruse K (June 1998). Inherited and de novo androgen receptor gene mutations: investigation of single-case families. J. Pediatr. 132 (6): 939—43. doi:10.1016/S0022-3476(98)70387-7. PMID 9627582.

Batch JA, Williams DM, Davies HR, Brown BD, Evans BA, Hughes IA, Patterson MN (October 1992). Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome. Hum. Mol. Genet. 1 (7): 497—503. doi:10.1093/hmg/1.7.497. PMID 1307250.

Hiort O, Klauber G, Cendron M, Sinnecker GH, Keim L, Schwinger E, Wolfe HJ, Yandell DW (May 1994). Molecular characterization of the androgen receptor gene in boys with hypospadias. Eur. J. Pediatr. 153 (5): 317—21. doi:10.1007/BF01956409. PMID 8033918. S2CID 12862106.

Lu J, Danielsen M (June 1996). A Stu I polymorphism in the human androgen receptor gene (AR). Clin. Genet. 49 (6): 323—4. doi:10.1111/j.1399-0004.1996.tb03800.x. PMID 8884086. S2CID 33645516.

Gottlieb B, Vasiliou DM, Lumbroso R, Beitel LK, Pinsky L, Trifiro MA (1999). Analysis of exon 1 mutations in the androgen receptor gene. Hum. Mutat. 14 (6): 527—39. doi:10.1002/(SICI)1098-1004(199912)14:6<527::AID-HUMU12>3.0.CO;2-X. PMID 10571951. S2CID 39155225.

Zuccarello D, Ferlin A, Vinanzi C, Prana E, Garolla A, Callewaert L, Claessens F, Brinkmann AO, Foresta C (April 2008). Detailed functional studies on androgen receptor mild mutations demonstrate their association with male infertility. Clin. Endocrinol. 68 (4): 580—8. doi:10.1111/j.1365-2265.2007.03069.x. PMID 17970778. S2CID 2783902.

Ferlin A, Vinanzi C, Garolla A, Selice R, Zuccarello D, Cazzadore C, Foresta C (November 2006). Male infertility and androgen receptor gene mutations: clinical features and identification of seven novel mutations. Clin. Endocrinol. 65 (5): 606—10. doi:10.1111/j.1365-2265.2006.02635.x. PMID 17054461. S2CID 33713391.

Stouffs K, Tournaye H, Liebaers I, Lissens W (2009). Male infertility and the involvement of the X chromosome. Hum. Reprod. Update. 15 (6): 623—37. doi:10.1093/humupd/dmp023. PMID 19515807.

Davis-Dao CA, Tuazon ED, Sokol RZ, Cortessis VK (November 2007). Male infertility and variation in CAG repeat length in the androgen receptor gene: a meta-analysis. J. Clin. Endocrinol. Metab. 92 (11): 4319—26. doi:10.1210/jc.2007-1110. PMID 17684052.

Kawate H, Wu Y, Ohnaka K, Tao RH, Nakamura K, Okabe T, Yanase T, Nawata H, Takayanagi R (November 2005). Impaired nuclear translocation, nuclear matrix targeting, and intranuclear mobility of mutant androgen receptors carrying amino acid substitutions in the deoxyribonucleic acid-binding domain derived from androgen insensitivity syndrome patients. J. Clin. Endocrinol. Metab. 90 (11): 6162—9. doi:10.1210/jc.2005-0179. PMID 16118342.

Sultan C, Paris F, Terouanne B, Balaguer P, Georget V, Poujol N, Jeandel C, Lumbroso S, Nicolas JC (2001). Disorders linked to insufficient androgen action in male children. Hum. Reprod. Update. 7 (3): 314—22. doi:10.1093/humupd/7.3.314. PMID 11392378.

nih.gov

pubmed.ncbi.nlm.nih.gov

Brown CJ, Goss SJ, Lubahn DB, Joseph DR, Wilson EM, French FS, Willard HF (February 1989). Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism. American Journal of Human Genetics. 44 (2): 264—9. PMC 1715398. PMID 2563196.

Hughes IA, Deeb A (December 2006). Androgen resistance. Best Pract. Res. Clin. Endocrinol. Metab. 20 (4): 577—98. doi:10.1016/j.beem.2006.11.003. PMID 17161333.

Lu J, Danielsen M (June 1996). A Stu I polymorphism in the human androgen receptor gene (AR). Clin. Genet. 49 (6): 323—4. doi:10.1111/j.1399-0004.1996.tb03800.x. PMID 8884086. S2CID 33645516.

Macke JP, Hu N, Hu S, Bailey M, King VL, Brown T, Hamer D, Nathans J (October 1993). Sequence variation in the androgen receptor gene is not a common determinant of male sexual orientation. American Journal of Human Genetics. 53 (4): 844—52. PMC 1682384. PMID 8213813.

Stouffs K, Tournaye H, Liebaers I, Lissens W (2009). Male infertility and the involvement of the X chromosome. Hum. Reprod. Update. 15 (6): 623—37. doi:10.1093/humupd/dmp023. PMID 19515807.

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

Lu J, Danielsen M (June 1996). A Stu I polymorphism in the human androgen receptor gene (AR). Clin. Genet. 49 (6): 323—4. doi:10.1111/j.1399-0004.1996.tb03800.x. PMID 8884086. S2CID 33645516.

Синдром Морріса (Ukrainian Wikipedia)

archive.org

doi.org

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

semanticscholar.org

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