Absence of mutations in the promoter and coding regions of STRA8 gene in patients with 46,XX disorders of gonadal development (2008)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidades: FM
- Subjects: MUTAÇÃO GENÉTICA; TRANSTORNOS GONADAIS; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Hormone Research
- Volume/Número/Paginação/Ano: v. 70, suppl. 1, p. 193, res. P2-d3-648, 2008
- Conference title: European Society for Paediatric Endocrinology (ESPE)
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ABNT
SANTOS, Mariza A. G.; NISHI, Mirian Y.; GOMES, Camila; et al. Absence of mutations in the promoter and coding regions of STRA8 gene in patients with 46,XX disorders of gonadal development. Hormone Research[S.l: s.n.], 2008. -
APA
Santos, M. A. G., Nishi, M. Y., Gomes, C., Domenice, S., Mendonça, B. B., & Costa, E. M. F. (2008). Absence of mutations in the promoter and coding regions of STRA8 gene in patients with 46,XX disorders of gonadal development. Hormone Research. Basel. -
NLM
Santos MAG, Nishi MY, Gomes C, Domenice S, Mendonça BB, Costa EMF. Absence of mutations in the promoter and coding regions of STRA8 gene in patients with 46,XX disorders of gonadal development. Hormone Research. 2008 ; 70 193. -
Vancouver
Santos MAG, Nishi MY, Gomes C, Domenice S, Mendonça BB, Costa EMF. Absence of mutations in the promoter and coding regions of STRA8 gene in patients with 46,XX disorders of gonadal development. Hormone Research. 2008 ; 70 193. - Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
- Crescimento linear e estatura final em crianças com tumores adrenais predominantemente virilizantes
- Absense of inactivating mutations and deletions of DAX1 gene in SRY negative 46,XX sex-reversed patients
- Absense of duplication on DAX1 gene in patients with 46,XY sex reversal
- Heterogeneidade clínica e molecular do hipogonadismo hipogonadotrófico (HH): importância da avaliação do sistema olfatório no diagnóstico diferencial
- Number of CAG repeats in Exon 1 of androgen receptor gene is not related to gender identity in adult patients with male psudohermaphroditism and male transexualism
- Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitibity syndrome in a brazilian cohort: five novel mutations in the androgen receptor gene
- Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
- Mutations in the SRY, DAX1, SF1 and WNT4 genes in brazilian sex-reversed patients
- Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty
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