The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants (2011)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- DOI: 10.1159/000316536
- Subjects: MUTAÇÃO GENÉTICA; TRANSTORNOS GONADAIS; CROMOSSOMOS SEXUAIS (FISIOPATOLOGIA)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Hormone Research in Paediatrics
- ISSN: 1663-2818
- Volume/Número/Paginação/Ano: v. 75, n. 1, p. 26-31, 2011
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
NISHI, Mirian Yumie et al. The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants. Hormone Research in Paediatrics, v. 75, n. 1, p. 26-31, 2011Tradução . . Disponível em: https://doi.org/10.1159/000316536. Acesso em: 19 abr. 2024. -
APA
Nishi, M. Y., Costa, E. M. F., Oliveira, S. B., Mendonca, B. B., & Domenice, S. (2011). The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants. Hormone Research in Paediatrics, 75( 1), 26-31. doi:10.1159/000316536 -
NLM
Nishi MY, Costa EMF, Oliveira SB, Mendonca BB, Domenice S. The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants [Internet]. Hormone Research in Paediatrics. 2011 ; 75( 1): 26-31.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1159/000316536 -
Vancouver
Nishi MY, Costa EMF, Oliveira SB, Mendonca BB, Domenice S. The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants [Internet]. Hormone Research in Paediatrics. 2011 ; 75( 1): 26-31.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1159/000316536 - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
- Absense of duplication on DAX1 gene in patients with 46,XY sex reversal
- 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
- 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
- Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
- Reavaliação na idade adulta do diagnóstico da deficiência de GH (DGH) determinado na infância
- Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty
Informações sobre o DOI: 10.1159/000316536 (Fonte: oaDOI API)
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