Author:
Raafat Shaymaa,Abdelmeguid Yasmine,Kotb Mostafa,Oshiba Ahmed
Publisher
Springer Science and Business Media LLC
Reference27 articles.
1. Ahmed S, Bashamboo A, Lucas-Herald A, McElreavey K. Understanding the genetic aetiology in patients with XY DSD. Br Med Bull. 2013;106:67–89.
2. Ahmed SF, Cheng A, Dovey L, et al. Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome. J Clin Endocrinol Metab. 2000;85:658–65.
3. Nixon R, Cerqueira V, Kyriakou A, et al. Prevalence of endocrine and genetic abnormalities in boys evaluated systematically for a disorder of sex development. Hum Reprod. 2017;32:2130–7.
4. Camats N, Fernández-Cancio M, Audí L, Schaller A, Flück CE. Broad phenotypes in heterozygous NR5A1 46, XY patients with a disorder of sex development: An oligogenic origin? Eur J Hum Genet. 2018;26:1329–38.
5. Baxter RM, Arboleda VA, Lee H, et al. Exome sequencing for the diagnosis of 46, XY disorders of sex development. J Clin Endocrinol Metab. 2015;100:E333–44.