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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 20819612)

  • 1. S578N mutation of the androgen receptor in an adolescent with complete androgen insensitivity syndrome.
    Xiao Y; Wang DF; Li XY; Yang J; Wang W
    Chin Med J (Engl); 2010 Jun; 123(11):1473-6. PubMed ID: 20819612
    [No Abstract]   [Full Text] [Related]  

  • 2. [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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. A novel androgen receptor gene mutation in a Chinese patient with complete androgen insensitivity syndrome.
    Sun S; Luo F; Zhou Z; Wu W
    Eur J Obstet Gynecol Reprod Biol; 2010 Dec; 153(2):173-5. PubMed ID: 20833465
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. [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]  

  • 10. [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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Human androgen insensitivity due to point mutations encoding amino acid substitutions in the androgen receptor steroid-binding domain.
    Murono K; Mendonca BB; Arnhold IJ; Rigon AC; Migeon CJ; Brown TR
    Hum Mutat; 1995; 6(2):152-62. PubMed ID: 7581399
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Molecular studies of a patient with complete androgen insensitivity and a 47,XXY karyotype.
    Girardin CM; Deal C; Lemyre E; Paquette J; Lumbroso R; Beitel LK; Trifiro MA; Van Vliet G
    J Pediatr; 2009 Sep; 155(3):439-43. PubMed ID: 19732585
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Androgen insensitivity syndrome (or Morris syndrome) and other associated pathologies.
    Dell'Edera D; Malvasi A; Vitullo E; Epifania AA; Tinelli A; Laterza F; Novelli A; Pacella E; Mazzone E; Novelli G
    Eur Rev Med Pharmacol Sci; 2010 Nov; 14(11):947-57. PubMed ID: 21284344
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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; 2003 Nov; 269(1):25-9. PubMed ID: 14605819
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Five novel androgen receptor gene mutations associated with complete androgen insensitivity syndrome.
    Jääskeläinen J; Mongan NP; Harland S; Hughes IA
    Hum Mutat; 2006 Mar; 27(3):291. PubMed ID: 16470553
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.