260 related articles for article (PubMed ID: 23450491)
1. [Identification of a novel frameshift mutation of human androgen receptor gene in a patient featuring complete androgen insensitivity syndrome].
Xie JH; Qu JH; Xiao QZ; Zhou YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):99-101. PubMed ID: 23450491
[TBL] [Abstract][Full Text] [Related]
2. 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]
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. 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]
5. Complete androgen insensitivity caused by a new frameshift deletion of two base pairs in exon 1 of the human androgen receptor gene.
Thiele B; Weidemann W; Schnabel D; Romalo G; Schweikert HU; Spindler KD
J Clin Endocrinol Metab; 1999 May; 84(5):1751-3. PubMed ID: 10323411
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. A novel nonsense mutation in the androgen receptor gene causes the complete androgen insensitivity syndrome.
Liu X; Fu J; Cai Z; Sun L; Zhang X; Li Z; Diao R; Wang Z; Yu G; Cai Z; Gui Y
J Androl; 2012; 33(3):357-60. PubMed ID: 21757511
[TBL] [Abstract][Full Text] [Related]
8. Analysis of exon 1 mutations in the androgen receptor gene.
Gottlieb B; Vasiliou DM; Lumbroso R; Beitel LK; Pinsky L; Trifiro MA
Hum Mutat; 1999; 14(6):527-39. PubMed ID: 10571951
[TBL] [Abstract][Full Text] [Related]
9. Molecular features and clinical phenotypes in androgen insensitivity syndrome in the absence and presence of androgen receptor gene mutations.
Holterhus PM; Werner R; Hoppe U; Bassler J; Korsch E; Ranke MB; Dörr HG; Hiort O
J Mol Med (Berl); 2005 Dec; 83(12):1005-13. PubMed ID: 16283146
[TBL] [Abstract][Full Text] [Related]
10. Androgen receptor gene mutation identified by PCR-SSCP and sequencing in 4 patients with complete androgen insensitivity syndrome.
Choi C; Kim KC; Kim HO; Cho SH; Lee JB; Kim IS; Park KK; Cho NH; Juhng SW
Arch Gynecol Obstet; 2000 Apr; 263(4):201-5. PubMed ID: 10834333
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. 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]
13. [Analysis of a novel mutation of AR gene in a patient featuring mild androgen insensitivity syndrome].
Zhang Y; Li W; Du J; Cao W; Lu G; Tan Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Apr; 31(2):219-22. PubMed ID: 24711036
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. A novel E153X point mutation in the androgen receptor gene in a patient with complete androgen insensitivity syndrome.
Copelli SB; Lumbroso S; Audran F; Pellizzari EH; Heinrich JJ; Cigorraga SB; Sultan C; Chemes HE
Asian J Androl; 1999 Jun; 1(1-2):73-7. PubMed ID: 11225909
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. Complete androgen insensitivity syndrome and discordant Müllerian remnants: two cases with novel mutation in the androgen receptor.
Güven A; Dursun F; Özkanlı S; Güçlüer B; Kuru Lİ
J Pediatr Endocrinol Metab; 2013; 26(9-10):909-14. PubMed ID: 23729616
[TBL] [Abstract][Full Text] [Related]
18. A double nucleotide insertion-induced frame-shift mutation of the androgen receptor gene in a familial complete androgen insensitivity syndrome.
Rong HL; Suzuki N; Imai A
Eur J Obstet Gynecol Reprod Biol; 2010 Jan; 148(1):53-5. PubMed ID: 19815331
[TBL] [Abstract][Full Text] [Related]
19. Novel androgen receptor gene mutations in Australian patients with complete androgen insensitivity syndrome.
MacLean HE; Ball EM; Rekaris G; Warne GL; Zajac JD
Hum Mutat; 2004 Mar; 23(3):287. PubMed ID: 14974091
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]