BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

287 related articles for article (PubMed ID: 17382127)

  • 1. Ethical and legal implications of genetic testing in androgen insensitivity syndrome.
    Berg JS; French SL; McCullough LB; Kleppe S; Sutton VR; Gunn SK; Karaviti LP
    J Pediatr; 2007 Apr; 150(4):434-8. PubMed ID: 17382127
    [No Abstract]   [Full Text] [Related]  

  • 2. A novel Arg615Ser mutation of androgen receptor DNA-binding domain in three 46,XY sisters with complete androgen insensitivity syndrome and bilateral inguinal hernia.
    Sharma V; Singh R; Thangaraj K; Jyothy A
    Fertil Steril; 2011 Feb; 95(2):804.e19-21. PubMed ID: 20888558
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 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. [Androgen insensitivity syndrome--testicular feminization--Morris syndrome. A surgical procedure in cases when a testis is found during herniotomy in a girl].
    Arstad C; Lendorf A
    Ugeskr Laeger; 1994 Nov; 156(47):7057-8. PubMed ID: 7817416
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. 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]  

  • 8. 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]  

  • 9. [Incomplete androgen insensitivity].
    Luczay A; Sólyom J; Hiort O; Szabó E; Dobos M; Jenovári Z; Fekete G
    Orv Hetil; 2006 Sep; 147(37):1805-7. PubMed ID: 17131800
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Testicular feminization syndrome (androgen insensitivity).
    Marshall DG; Valentine GH
    J Pediatr Surg; 1981 Aug; 16(4):465-70. PubMed ID: 7277140
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial complete androgen insensitivity syndrome with prostatic tissue and seminal vesicles.
    Tripathy K; Gouda K; Palai PK; Das L
    Arch Gynecol Obstet; 2010 Nov; 282(5):581-3. PubMed ID: 20602105
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Androgen resistance.
    Hughes IA; Deeb A
    Best Pract Res Clin Endocrinol Metab; 2006 Dec; 20(4):577-98. PubMed ID: 17161333
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Bilateral inguinal hernia in a female child.
    Gil AT; Salgado M
    BMJ Case Rep; 2014 Feb; 2014():. PubMed ID: 24503661
    [No Abstract]   [Full Text] [Related]  

  • 14. [Inguinal hernia in a young girl; sporadic manifestation of testicular feminization].
    Ubachs JM; Brink PR
    Ned Tijdschr Geneeskd; 1997 Oct; 141(43):2071-3. PubMed ID: 9550766
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Screening for complete androgen insensitivity syndrome in girls with inguinal hernia: parental insight.
    Georgiou R; Hall NJ; Stanton M
    Arch Dis Child; 2013 Apr; 98(4):316-7. PubMed ID: 23418035
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. [Total testicular feminization].
    Strebelow W
    Z Arztl Fortbild (Jena); 1973 Mar; 67(5):238-40. PubMed ID: 4715513
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 15.