Similar articles for PMID: 10690872

Year	Number of Results
1946	1
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2024	1

1

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. Ahmed SF, et al. J Clin Endocrinol Metab. 2000 Feb;85(2):658-65. doi: 10.1210/jcem.85.2.6337. J Clin Endocrinol Metab. 2000. PMID: 10690872

2

Correlation between genotype, phenotype and sex of rearing in 111 patients with partial androgen insensitivity syndrome.

Deeb A, Mason C, Lee YS, Hughes IA. Deeb A, et al. Clin Endocrinol (Oxf). 2005 Jul;63(1):56-62. doi: 10.1111/j.1365-2265.2005.02298.x. Clin Endocrinol (Oxf). 2005. PMID: 15963062

3

Androgen insensitivity syndrome: somatic mosaicism of the androgen receptor in seven families and consequences for sex assignment and genetic counseling.

Köhler B, Lumbroso S, Leger J, Audran F, Grau ES, Kurtz F, Pinto G, Salerno M, Semitcheva T, Czernichow P, Sultan C. Köhler B, et al. J Clin Endocrinol Metab. 2005 Jan;90(1):106-11. doi: 10.1210/jc.2004-0462. Epub 2004 Nov 2. J Clin Endocrinol Metab. 2005. PMID: 15522944

4

Clinical, hormonal and genetic characteristics of androgen insensitivity syndrome in 39 Chinese patients.

Liu Q, Yin X, Li P. Liu Q, et al. Reprod Biol Endocrinol. 2020 Apr 28;18(1):34. doi: 10.1186/s12958-020-00593-0. Reprod Biol Endocrinol. 2020. PMID: 32345305 Free PMC article.

5

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. Boehmer AL, et al. J Clin Endocrinol Metab. 2001 Sep;86(9):4151-60. doi: 10.1210/jcem.86.9.7825. J Clin Endocrinol Metab. 2001. PMID: 11549642 Free article.

6

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. Raicu F, et al. Asian J Androl. 2008 Jul;10(4):687-91. doi: 10.1111/j.1745-7262.2008.00376.x. Epub 2007 Dec 20. Asian J Androl. 2008. PMID: 18097502 Free article.

7

AR mutations in 28 patients with androgen insensitivity syndrome (Prader grade 0-3).

Wang Y, Gong C, Wang X, Qin M. Wang Y, et al. Sci China Life Sci. 2017 Jul;60(7):700-706. doi: 10.1007/s11427-017-9084-9. Epub 2017 Jun 14. Sci China Life Sci. 2017. PMID: 28624954

8

Partial androgen insensitivity syndrome with R840H mutation in androgen receptor: report of one case.

Yen JL, Chang KH, Sheu JC, Lee YJ, Tsai LP. Yen JL, et al. Acta Paediatr Taiwan. 2005 Mar-Apr;46(2):101-5. Acta Paediatr Taiwan. 2005. PMID: 16302589

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. Ledig S, et al. Horm Res. 2005;63(6):263-9. doi: 10.1159/000086018. Epub 2005 May 26. Horm Res. 2005. PMID: 15925895

10

Analysis of exon 1 mutations in the androgen receptor gene.

Gottlieb B, Vasiliou DM, Lumbroso R, Beitel LK, Pinsky L, Trifiro MA. Gottlieb B, et al. Hum Mutat. 1999;14(6):527-39. doi: 10.1002/(SICI)1098-1004(199912)14:6<527::AID-HUMU12>3.0.CO;2-X. Hum Mutat. 1999. PMID: 10571951

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