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Journal Abstract Search

293 related items for PubMed ID: 28456808

  • 21. 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
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  • 22. Somatic mosaicism of androgen receptor gene in an androgen insensitivity syndrome patient conceived through assisted reproduction technique.
    Wang H, Zhu H, Wang N, Cheng T, Han B, Zhao S, Song H, Cheng K, Liu Y, Qiao J.
    Mol Genet Genomic Med; 2019 Oct; 7(10):e00906. PubMed ID: 31429517
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  • 25. A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty.
    Koçyiğit C, Sarıtaş S, Çatlı G, Onay H, Dündar BN.
    J Clin Res Pediatr Endocrinol; 2016 Jun 05; 8(2):232-5. PubMed ID: 27087292
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  • 26. A novel mutation (c.T3816 > C) in the androgen receptor gene in a 46,XY female patient with androgen insensitivity syndrome.
    Helszer Z, Dmochowska A, Borkowska E, Moczulska H, Słowikowska-Hilczer J, Pietrusiński M, Jędrzejczyk S, Kałużewski B.
    Endokrynol Pol; 2013 Jun 05; 64(5):398-402. PubMed ID: 24186597
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  • 27. Complete androgen insensitivity syndrome caused by a novel mutation in the ligand-binding domain of the androgen receptor: functional characterization.
    Rosa S, Biason-Lauber A, Mongan NP, Navratil F, Schoenle EJ.
    J Clin Endocrinol Metab; 2002 Sep 05; 87(9):4378-82. PubMed ID: 12213902
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  • 28. 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 Sep 05; 33(3):357-60. PubMed ID: 21757511
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  • 30.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Gottlieb B, Trifiro MA.
    ; 1993 Sep 05. PubMed ID: 20301602
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  • 31. [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 05; 43(11):828-30. PubMed ID: 19087565
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  • 32. 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 Nov 05; 45(6):342-5. PubMed ID: 11185742
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  • 35. 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 05; 153(2):173-5. PubMed ID: 20833465
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  • 36. Novel molecular defects in the androgen receptor gene of Mexican patients with androgen insensitivity.
    Chávez B, Vilchis F, Zenteno JC, Larrea F, Kofman-Alfaro S.
    Clin Genet; 2001 Mar 05; 59(3):185-8. PubMed ID: 11260228
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  • 37. Genetic diagnosis and genetic counseling for androgen-insensitivity syndrome: a report of three cases.
    Yamaguchi M, Sameshima H, Ikenoue T.
    J Obstet Gynaecol Res; 2014 Mar 05; 40(3):723-7. PubMed ID: 24321103
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  • 38. New mutation causing androgen insensitivity syndrome - a case report and review of literature.
    Maciejewska-Jeske M, Rojewska-Madziala P, Broda K, Drabek K, Szeliga A, Czyzyk A, Malinger S, Kostrzak A, Podfigurna A, Bala G, Meczekalski B, Malcher A, Kurpisz M.
    Gynecol Endocrinol; 2019 Apr 05; 35(4):294-297. PubMed ID: 30449224
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  • 39. A recurrent synonymous mutation in the human androgen receptor gene causing complete androgen insensitivity syndrome.
    Batista RL, Rodrigues ADS, Nishi MY, Gomes NL, Faria JAD, Moraes DR, Carvalho LR, Costa EMF, Domenice S, Mendonca BB.
    J Steroid Biochem Mol Biol; 2017 Nov 05; 174():14-16. PubMed ID: 28743543
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  • 40. [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 05; 56(4):347-52. PubMed ID: 11927080
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