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The Use of Genetics for Reaching a Diagnosis in XY DSD.
Ahmed SF, Alimusina M, Batista RL, Domenice S, Lisboa Gomes N, McGowan R, Patjamontri S, Mendonca BB. Ahmed SF, et al. Among authors: mendonca bb. Sex Dev. 2022;16(2-3):207-224. doi: 10.1159/000524881. Epub 2022 May 30. Sex Dev. 2022. PMID: 35636390 Free article. Review.
46,XY disorders of sex development (DSD).
Mendonca BB, Domenice S, Arnhold IJ, Costa EM. Mendonca BB, et al. Clin Endocrinol (Oxf). 2009 Feb;70(2):173-87. doi: 10.1111/j.1365-2265.2008.03392.x. Clin Endocrinol (Oxf). 2009. PMID: 18811725 Review.
[Absence of PRKAR1A loss of heterozygosity in laser-captured microdissected pigmented nodular adrenocortical tissue from a patient with Carney complex caused by the novel nonsense mutation p.Y21X].
Almeida MQ, Brito LP, Domenice S, Costa MH, Pinto EM, Osório CA, Latronico AC, Mendonca BB, Fragoso MC. Almeida MQ, et al. Among authors: mendonca bb. Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1257-63. doi: 10.1590/s0004-27302008000800009. Arq Bras Endocrinol Metabol. 2008. PMID: 19169478 Portuguese.
491 results