211 related articles for article (PubMed ID: 21710452)
1. Clinical and genetic characterization of complete androgen insensitivity syndrome in a Chinese family.
Li BK; Ding Q; Wan XD; Wang X
Genet Mol Res; 2011 May; 10(2):1022-31. PubMed ID: 21710452
[TBL] [Abstract][Full Text] [Related]
2. [Replacement of androgen receptor gene causes complete androgen insensitivity in a large family].
Qin YY; Gao X; You L; Li Y; Yan JH; Zhao YR; Chen ZJ
Zhonghua Fu Chan Ke Za Zhi; 2008 Nov; 43(11):828-30. PubMed ID: 19087565
[TBL] [Abstract][Full Text] [Related]
3. A large deletion/insertion-induced frameshift mutation of the androgen receptor gene in a family with a familial complete androgen insensitivity syndrome.
Cong P; Ye Y; Wang Y; Lu L; Yong J; Yu P; Joseph KK; Jin F; Qi M
Gene; 2012 Jun; 500(2):220-3. PubMed ID: 22487869
[TBL] [Abstract][Full Text] [Related]
4. Identification of a critical novel mutation in the exon 1 of androgen receptor gene in 2 brothers with complete androgen insensitivity syndrome.
Radpour R; Falah M; Aslani A; Zhong XY; Saleki A
J Androl; 2009; 30(3):230-2. PubMed ID: 19023143
[TBL] [Abstract][Full Text] [Related]
5. [Deletion of thymine at position 2298 in exon 5 of the androgenic receptor gene causing complete androgen insensitivity syndrome].
Soriano Guillén L; Muñoz Calvo MT; Martinez Pérez J; Pozo Román J; Martín Sobrino MA; González Medeiro I; Argente Oliver J
An Esp Pediatr; 2002 Apr; 56(4):347-52. PubMed ID: 11927080
[TBL] [Abstract][Full Text] [Related]
6. Leu-676-Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred.
Belsham DD; Pereira F; Greenberg CR; Liao S; Wrogemann K
Hum Mutat; 1995; 5(1):28-33. PubMed ID: 7537149
[TBL] [Abstract][Full Text] [Related]
7. Molecular analysis of familial androgen insensitivity syndrome due to replacement of glutamic acid 802 by lysine.
Sawai H; Komori S; Sakata K; Nakae K; Shima H; Matsumoto F; Matsumoto H; Onishi Y; Okada Y; Yoshida O; Koyama K
J Hum Genet; 2000; 45(6):342-5. PubMed ID: 11185742
[TBL] [Abstract][Full Text] [Related]
8. Identification of a mutant allele of the androgen receptor gene in a family with androgen insensitivity syndrome: detection of carriers and prenatal diagnosis.
Fogu G; Bertini V; Dessole S; Bandiera P; Campus PM; Capobianco G; Sanna R; Soro G; Montella A
Arch Gynecol Obstet; 2004 May; 269(4):266-9. PubMed ID: 12898143
[TBL] [Abstract][Full Text] [Related]
9. A practical approach to the detection of androgen receptor gene mutations and pedigree analysis in families with x-linked androgen insensitivity.
Ris-Stalpers C; Hoogenboezem T; Sleddens HF; Verleun-Mooijman MC; Degenhart HJ; Drop SL; Halley DJ; Oosterwijk JC; Hodgins MB; Trapman J
Pediatr Res; 1994 Aug; 36(2):227-34. PubMed ID: 7970939
[TBL] [Abstract][Full Text] [Related]
10. Eight novel mutations of the androgen receptor gene in patients with androgen insensitivity syndrome.
Chávez B; Méndez JP; Ulloa-Aguirre A; Larrea F; Vilchis F
J Hum Genet; 2001; 46(10):560-5. PubMed ID: 11587068
[TBL] [Abstract][Full Text] [Related]
11. [Mutation analysis of the androgen receptor gene in a complete androgen insensitivity syndrome family].
Wu W; Luo F; Geng Q; Hao Y; Chen W; Cai J; Xie J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):606-9. PubMed ID: 19953479
[TBL] [Abstract][Full Text] [Related]
12. Double-strand DNA break repair with replication slippage on two strands: a novel mechanism of deletion formation.
MacLean HE; Favaloro JM; Warne GL; Zajac JD
Hum Mutat; 2006 May; 27(5):483-9. PubMed ID: 16619235
[TBL] [Abstract][Full Text] [Related]
13. A mutation c.C2812T in the androgen receptor gene resulting in Pro817Leu substitution may affect dimerization of the androgen receptor and result in androgen insensitivity syndrome.
Turek-Plewa J; Eckersdorf-Mastalerz A; Kaluzewski B; Helszer Z; Trzeciak WH
Fertil Steril; 2006 Jun; 85(6):1822.e1-4. PubMed ID: 16759930
[TBL] [Abstract][Full Text] [Related]
14. Related individuals with different androgen receptor gene deletions.
MacLean HE; Chu S; Warne GL; Zajac JD
J Clin Invest; 1993 Mar; 91(3):1123-8. PubMed ID: 8450042
[TBL] [Abstract][Full Text] [Related]
15. Partial androgen insensitivity syndrome with R840H mutation in androgen receptor: report of one case.
Yen JL; Chang KH; Sheu JC; Lee YJ; Tsai LP
Acta Paediatr Taiwan; 2005; 46(2):101-5. PubMed ID: 16302589
[TBL] [Abstract][Full Text] [Related]
16. Characterization of a novel receptor mutation A-->T at exon 4 in complete androgen insensitivity syndrome and a carrier sibling via bidirectional polymorphism sequence analysis.
Sills ES; Sholes TE; Perloe M; Kaplan CR; Davis JG; Tucker MJ
Int J Mol Med; 2002 Jan; 9(1):45-8. PubMed ID: 11744994
[TBL] [Abstract][Full Text] [Related]
17. Novel and recurrent mutations in patients with androgen insensitivity syndromes.
Ledig S; Jakubiczka S; Neulen J; Aulepp U; Burck-Lehmann U; Mohnike K; Thiele H; Zierler H; Brewer C; Wieacker P
Horm Res; 2005; 63(6):263-9. PubMed ID: 15925895
[TBL] [Abstract][Full Text] [Related]
18. A novel mutation in the CAG triplet region of exon 1 of androgen receptor gene causes complete androgen insensitivity syndrome in a large kindred.
Zhu YS; Cai LQ; Cordero JJ; Canovatchel WJ; Katz MD; Imperato-McGinley J
J Clin Endocrinol Metab; 1999 May; 84(5):1590-4. PubMed ID: 10323385
[TBL] [Abstract][Full Text] [Related]
19. [A novel mutation Glu441stop (GAA to TAA) of androgen receptor gene resulting in complete androgen insensitivity syndrome].
LUO FW; WU WQ; GENG Q; LI F; CHEN WB; GAN WX; XIE JS
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):176-9. PubMed ID: 21462130
[TBL] [Abstract][Full Text] [Related]
20. [An acceptor-splice-site mutation responsible for complete androgen insensitivity syndrome].
Zhang W; Li X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):14-6. PubMed ID: 11172634
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]