BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

80 related articles for article (PubMed ID: 22332610)

  • 1. Preimplantation and prenatal genetic diagnosis for androgen insensitivity syndrome resulting from a novel deletion/insertion mutation.
    Ye Y; Cong P; Yu P; Qi M; Jin F
    Clin Genet; 2012 Sep; 82(3):295-6. PubMed ID: 22332610
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. [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]  

  • 5. Prenatal diagnosis of androgen insensitivity syndrome.
    Bianca S; Cataliotti A; Bartoloni G; Torrente I; Barrano B; Boemi G; Lo Presti M; Indaco L; Barone C; Ettore G
    Fetal Diagn Ther; 2009; 26(3):167-9. PubMed ID: 19844078
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Complete Androgen Insensitivity Syndrome: A Rare Case of Prenatal Diagnosis.
    Coelho ML; Soares E; Freixo M; Brandão P; Marinho C; Rocha J; Rodrigues G
    Rev Bras Ginecol Obstet; 2021 Sep; 43(9):710-712. PubMed ID: 34670306
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [From gene to disease; androgen receptor gene, androgen insensitivity syndrome, and spinal and bulbar muscle atrophy].
    Boehmer AL; Brinkmann AO; Niermeijer MF; Halley DJ; Drop SL
    Ned Tijdschr Geneeskd; 2001 Dec; 145(48):2326-8. PubMed ID: 11766302
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. 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]  

  • 10. Novel human pathological mutations. Gene symbol: AR. Disease: androgen insensitivity syndrome.
    Turek-Plewa J; Jerzy S; Wieslaw HT
    Hum Genet; 2009 Apr; 125(3):341. PubMed ID: 19309788
    [No Abstract]   [Full Text] [Related]  

  • 11. [Androgen insensitivity syndrome].
    Giwercman YL; Svensson J
    Tidsskr Nor Laegeforen; 2008 Feb; 128(5):581-5. PubMed ID: 18311203
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Long-term followup and comparison between genotype and phenotype in 29 cases of complete androgen insensitivity syndrome.
    Cheikhelard A; Morel Y; Thibaud E; Lortat-Jacob S; Jaubert F; Polak M; Nihoul-Fekete C
    J Urol; 2008 Oct; 180(4):1496-501. PubMed ID: 18710728
    [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. Novel androgen receptor gene mutation in patient with complete androgen insensitivity syndrome.
    Ning Y; Zhang F; Zhu Y; Chen H; Lu J; Li Z
    Urology; 2012 Jul; 80(1):216-8. PubMed ID: 22608796
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [Differential diagnosis and treatment of girls with 46XY-karyotype and androgen insensitivity syndrome].
    Drop SL; Boehmer AL; Slijper FM; Nijman JM; Hazebroek FW; Niermeijer MF
    Ned Tijdschr Geneeskd; 2001 Apr; 145(14):665-9. PubMed ID: 11530701
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Healthy birth after testicular extraction of sperm and ICSI from an azoospermic man with mild androgen insensitivity syndrome caused by an androgen receptor partial loss-of-function mutation.
    Massin N; Bry H; Vija L; Maione L; Constancis E; Haddad B; Morel Y; Claessens F; Young J
    Clin Endocrinol (Oxf); 2012 Oct; 77(4):593-8. PubMed ID: 22469007
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Discordant embryonic aneuploidy testing and prenatal ultrasonography prompting androgen insensitivity syndrome diagnosis.
    Franasiak JM; Yao X; Ashkinadze E; Rosen T; Scott RT
    Obstet Gynecol; 2015 Feb; 125(2):383-386. PubMed ID: 25569013
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.