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Journal Abstract Search

209 related items for PubMed ID: 15813610

  • 1. Complete androgen insensitivity syndrome caused by the R855H mutation in the androgen receptor gene.
    Skordis N, Lumbroso S, Perikleous M, Sismani C, Patsalis PC, Sultan C.
    J Pediatr Endocrinol Metab; 2005 Mar; 18(3):309-13. PubMed ID: 15813610
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  • 2. Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome.
    Ahmed SF, Cheng A, Dovey L, Hawkins JR, Martin H, Rowland J, Shimura N, Tait AD, Hughes IA.
    J Clin Endocrinol Metab; 2000 Feb; 85(2):658-65. PubMed ID: 10690872
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  • 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
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  • 5. 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
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  • 6. Genotype versus phenotype in families with androgen insensitivity syndrome.
    Boehmer AL, Brinkmann O, Brüggenwirth H, van Assendelft C, Otten BJ, Verleun-Mooijman MC, Niermeijer MF, Brunner HG, Rouwé CW, Waelkens JJ, Oostdijk W, Kleijer WJ, van der Kwast TH, de Vroede MA, Drop SL.
    J Clin Endocrinol Metab; 2001 Sep; 86(9):4151-60. PubMed ID: 11549642
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  • 7. 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
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  • 8. Clinical characteristics and molecular genetics of complete androgen insensitivity syndrome patients: a series study of 30 cases from a Chinese tertiary medical center.
    Zhang D, Yao F, Tian T, Deng S, Luo M, Tian Q.
    Fertil Steril; 2021 May; 115(5):1270-1279. PubMed ID: 33602557
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  • 13. Three novel and two known androgen receptor gene mutations associated with androgen insensitivity syndrome in sex-reversed XY female patients.
    Saranya B, Bhavani G, Arumugam B, Jayashankar M, Santhiya ST.
    J Genet; 2016 Dec; 95(4):911-921. PubMed ID: 27994190
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  • 15. A novel mutation of the androgen receptor gene in familial complete androgen insensitivity syndrome.
    Li Y, Qu S, Li P.
    Eur Rev Med Pharmacol Sci; 2015 Nov; 19(21):4146-52. PubMed ID: 26592841
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  • 16. [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
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  • 17. Point mutations detected in the androgen receptor gene of three men with partial androgen insensitivity syndrome.
    Saunders PT, Padayachi T, Tincello DG, Shalet SM, Wu FC.
    Clin Endocrinol (Oxf); 1992 Sep; 37(3):214-20. PubMed ID: 1424203
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  • 18. Heterozygous Nonsense Mutation in the Androgen Receptor Gene Associated with Partial Androgen Insensitivity Syndrome in an Individual with 47,XXY Karyotype.
    Batista RL, Rodrigues AS, Nishi MY, Feitosa ACR, Gomes NLRA, Junior JAF, Domenice S, Costa EMF, de Mendonça BB.
    Sex Dev; 2017 Sep; 11(2):78-81. PubMed ID: 28456808
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  • 20. Prenatal Diagnosis of Twin Fetuses with a Novel AR Gene Mutation in a Chinese Family of Complete Androgen Insensitivity Syndrome.
    Wu W, Geng Q, Liu Y, Xu Z, Li P, Xie J.
    Fetal Pediatr Pathol; 2017 Dec; 36(6):432-436. PubMed ID: 29206494
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