Coriocarcinoma en un hermafrodita verdadero 46, XY
Arvelo, Nelson; Rivas, Janet Ivonne; Abud Alberto, Kahwaty; Velásquez, Luz Marina; Durán, María Cristina.
Rev. venez. cir
; 51(1/2): 44-48, ene.-jun. 1998. ilus
Artigo em Espanhol | LILACS | ID: lil-305362
Severe combined adrenal and gonadal deficiency caused by novel mutations in the cholesterol side chain cleavage enzyme, P450scc.
Description of diagnosis of 45,X/46,XY ovotesticular DSD.
[Children born with ambiguous genitalia].
A Unique Presentation of XY Gonadal Dysgenesis in Frasier Syndrome due to WT1 Mutation and a Literature Review.
A novel SRY gene mutation c.266 A>T (p.E89V) in a 46,XY complete gonadal dysgenesis patient.
SUBMICROSCOPIC DUPLICATION OF 8q24.3 REGION IS A POTENTIAL CANDIDATE FOR DISORDERS OF SEX DEVELOPMENT.
Mutations in MAP3K1 that cause 46,XY disorders of sex development disrupt distinct structural domains in the protein.
Sexual quality of life of individuals with disorders of sex development and a 46,XY karyotype: a review of international research.
Gonadal tumour risk in 292 phenotypic female patients with disorders of sex development containing Y chromosome or Y-derived sequence.
Hormonal evaluation in relation to phenotype and genotype in 286 patients with a disorder of sex development from Indonesia.