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B. K. Li, Ding, Q., Wan, X. D., and Wang, X., Clinical and genetic characterization of complete androgen insensitivity syndrome in a Chinese family, vol. 10, pp. 1022-1031, 2011.
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Molecular basis of androgen insensitivity. Mol. Cell. Endocrinol. 179: 105-109. doi:10.1016/S0303-7207(01)00466-X Cheikhelard A, Morel Y, Thibaud E, Lortat-Jacob S, et al. (2008). Long-term followup and comparison between genotype and phenotype in 29 cases of complete androgen insensitivity syndrome. J. Urol. 180: 1496-1501. doi:10.1016/j.juro.2008.06.045 PMid:18710728 Cools M, Looijenga LH, Wolffenbuttel KP and Drop SL (2009). Disorders of sex development: update on the genetic background, terminology and risk for the development of germ cell tumors. World J. Pediatr. 5: 93-102. doi:10.1007/s12519-009-0020-7 PMid:19718530 Fogu G, Bertini V, Dessole S, Bandiera P, et al. (2003). Identification of a mutant allele of the androgen receptor gene in a family with androgen insensitivity syndrome: detection of carriers and prenatal diagnosis. Arch. Gynecol. Obstet. 269: 25-29. doi:10.1007/s00404-002-0386-4 PMid:14605819 Gottlieb B, Beitel LK, Wu JH and Trifiro M (2004). 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Study of bone mineral density in complete androgen insensitivity syndrome patients. Zhonghua Fu Chan Ke Za Zhi 40: 799-802. PMid:16412322 Ulloa-Aguirre A, Carranza-Lira S, Mendez JP, Angeles A, et al. (1990). Incomplete regression of mullerian ducts in the androgen insensitivity syndrome. Fertil. Steril. 53: 1024-1028. PMid:2112490 Wilson JD, Leihy MW, Shaw G and Renfree MB (2002). Androgen physiology: unsolved problems at the millennium. Mol. Cell. Endocrinol. 198: 1-5. doi:10.1016/S0303-7207(02)00362-3