Nongenetic male pseudohermaphroditism and reduced prenatal growth (2001)
- Authors:
- Autor USP: MENDONCA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Assunto: HERMAFRODITISMO
- Language: Inglês
- Imprenta:
- Publisher place: Reino Unido
- Date published: 2001
- Source:
- Título do periódico: The New England Journal of Medicine
- ISSN: 0028-4793
- Volume/Número/Paginação/Ano: v. 345, n. 15, p. 1135, october 2001
-
ABNT
MENDONÇA, Berenice B. e BILLERBECK, Ana Elisa C. Nongenetic male pseudohermaphroditism and reduced prenatal growth. The New England Journal of Medicine, v. 345, n. 15, p. 1135, 2001Tradução . . Acesso em: 24 abr. 2024. -
APA
Mendonça, B. B., & Billerbeck, A. E. C. (2001). Nongenetic male pseudohermaphroditism and reduced prenatal growth. The New England Journal of Medicine, 345( 15), 1135. -
NLM
Mendonça BB, Billerbeck AEC. Nongenetic male pseudohermaphroditism and reduced prenatal growth. The New England Journal of Medicine. 2001 ; 345( 15): 1135.[citado 2024 abr. 24 ] -
Vancouver
Mendonça BB, Billerbeck AEC. Nongenetic male pseudohermaphroditism and reduced prenatal growth. The New England Journal of Medicine. 2001 ; 345( 15): 1135.[citado 2024 abr. 24 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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- 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
- Microconversão no promotor do gene CYP21A2 envolvendo os sítios de ligação dos fatores de transcrição Sp1 e ASP: nova etiologia molecular da deficiência de 21-hidroxilase (21OHD)
- Three novel mutations in CYP21 gene in brazilian patients with the classical form of 21-hydroxylase deficiency due to founder effect
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