Reply to correspondence from hall - "detection of Y-specific sequences in patients with turner syndrome" (2002)
- Autores:
- Autores USP: MENDONCA, BERENICE BILHARINHO DE - FM ; DOMENICE, SORAHIA - FM
- Unidade: FM
- Assuntos: GENÉTICA; ENDOCRINOLOGIA
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: n. 107
-
ABNT
NISHI, Miriam et al. Reply to correspondence from hall - "detection of Y-specific sequences in patients with turner syndrome". American Journal of Medical Genetics. New York: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 abr. 2024. , 2002 -
APA
Nishi, M., Domenice, S., Medeiros, M. A., Mendonça, B. B., & Billerbeck, A. E. C. (2002). Reply to correspondence from hall - "detection of Y-specific sequences in patients with turner syndrome". American Journal of Medical Genetics. New York: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Nishi M, Domenice S, Medeiros MA, Mendonça BB, Billerbeck AEC. Reply to correspondence from hall - "detection of Y-specific sequences in patients with turner syndrome". American Journal of Medical Genetics. 2002 ;( 107):[citado 2024 abr. 24 ] -
Vancouver
Nishi M, Domenice S, Medeiros MA, Mendonça BB, Billerbeck AEC. Reply to correspondence from hall - "detection of Y-specific sequences in patients with turner syndrome". American Journal of Medical Genetics. 2002 ;( 107):[citado 2024 abr. 24 ] - Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
- 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
- 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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