These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
110 related articles for article (PubMed ID: 29693241)
21. Complete androgen insensitivity syndrome in juveniles and adults with female phenotypes. Wang Z; Sa YL; Ye XX; Zhang J; Xu YM J Obstet Gynaecol Res; 2014 Sep; 40(9):2044-50. PubMed ID: 25170741 [TBL] [Abstract][Full Text] [Related]
22. A missense mutation in the androgen receptor gene causing androgen insensitivity syndrome in a Chinese family. Li L; Liu WM; Liu MX; Zheng SQ; Zhang JX; Che FY; Liu SG Asian J Androl; 2017; 19(2):260-261. PubMed ID: 26806084 [No Abstract] [Full Text] [Related]
23. A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome. Yuan SM; Huang H; Tu CF; Du J; Xu DB; Lin G; Lu GX; Tan YQ Asian J Androl; 2018; 20(3):308-310. PubMed ID: 28857053 [No Abstract] [Full Text] [Related]
24. Novel mutation in the ligand-binding domain of the androgen receptor gene (l790p) associated with complete androgen insensitivity syndrome. Raicu F; Giuliani R; Gatta V; Palka C; Franchi PG; Lelli-Chiesa P; Tumini S; Stuppia L Asian J Androl; 2008 Jul; 10(4):687-91. PubMed ID: 18097502 [TBL] [Abstract][Full Text] [Related]
25. Mutations of the androgen receptor gene in patients with complete androgen insensitivity. Jakubiczka S; Nedel S; Werder EA; Schleiermacher E; Theile U; Wolff G; Wieacker P Hum Mutat; 1997; 9(1):57-61. PubMed ID: 8990010 [No Abstract] [Full Text] [Related]
26. A novel arg616Cys mutation in the DNA-binding domain of complete androgen insensitivity syndrome in a Chinese family. Zhou L; Wang CH Chin Med J (Engl); 2013 Nov; 126(21):4192-3. PubMed ID: 24229697 [No Abstract] [Full Text] [Related]
28. 46,XY disorders of sex development--the undermasculinised male with disorders of androgen action. Werner R; Grötsch H; Hiort O Best Pract Res Clin Endocrinol Metab; 2010 Apr; 24(2):263-77. PubMed ID: 20541151 [TBL] [Abstract][Full Text] [Related]
29. Molecular analysis of the androgen receptor gene in 4 patients with complete androgen insensitivity. Komori S; Kasumi H; Sakata K; Tanaka H; Hamada K; Koyama K Arch Gynecol Obstet; 1998; 261(2):95-100. PubMed ID: 9544375 [TBL] [Abstract][Full Text] [Related]
30. Androgens and fetal growth. de Zegher F; Francois I; Boehmer AL; Saggese G; Müller J; Hiort O; Sultan C; Clayton P; Brauner R; Cacciari E; Ibáñez L; Van Vliet G; Tiulpakov A; Saka N; Ritzén M; Sippell WG Horm Res; 1998; 50(4):243-4. PubMed ID: 9838248 [TBL] [Abstract][Full Text] [Related]
31. A novel point mutation (R840S) in the androgen receptor in a Brazilian family with partial androgen insensitivity syndrome. Melo KF; Latronico AC; Costa EM; Billerbeck AE; Mendonca BB; Arnhold IJ Hum Mutat; 1999 Oct; 14(4):353. PubMed ID: 10502786 [TBL] [Abstract][Full Text] [Related]
32. Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitivity syndrome in a Brazilian cohort: five novel mutations in the androgen receptor gene. Melo KF; Mendonca BB; Billerbeck AE; Costa EM; Inácio M; Silva FA; Leal AM; Latronico AC; Arnhold IJ J Clin Endocrinol Metab; 2003 Jul; 88(7):3241-50. PubMed ID: 12843171 [TBL] [Abstract][Full Text] [Related]
38. Phenotypic and molecular characteristics of androgen insensitivity syndrome patients. Yuan SM; Zhang YN; Du J; Li W; Tu CF; Meng LL; Lin G; Lu GX; Tan YQ Asian J Androl; 2018; 20(5):473-478. PubMed ID: 29785970 [TBL] [Abstract][Full Text] [Related]
39. Androgen insensitivity syndrome: somatic mosaicism of the androgen receptor in seven families and consequences for sex assignment and genetic counseling. Köhler B; Lumbroso S; Leger J; Audran F; Grau ES; Kurtz F; Pinto G; Salerno M; Semitcheva T; Czernichow P; Sultan C J Clin Endocrinol Metab; 2005 Jan; 90(1):106-11. PubMed ID: 15522944 [TBL] [Abstract][Full Text] [Related]
40. A novel nonsense mutation in the N-terminal domain of the androgen receptor gene causes complete androgen insensitivity syndrome. Cai Z; Li ZS; Liu XY J Obstet Gynaecol; 2012 Oct; 32(7):707-8. PubMed ID: 22943730 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]