Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue (2001)
- Authors:
- USP affiliated authors: MENDONCA, BERENICE BILHARINHO DE - FM ; DOMENICE, SORAHIA - FM ; CARVALHO, FILOMENA MARINO - FM ; LATRONICO, ANA CLAUDIA - FM ; ARNHOLD, IVO JORGE PRADO - FM
- Unidades: FM; FM; FM; FM; FM
- Subjects: ENDOCRINOLOGIA; HORMÔNIOS; GENÉTICA MOLECULAR
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Medical Science Monitor
- Volume/Número/Paginação/Ano: v. 7, n. 2, p. 238-241, 2001
-
ABNT
DOMENICE, Sorahia; NISHI, Miriam Yumie; BILLERBECK, Ana Elisa Correia; et al. Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue. Medical Science Monitor, Thorofare, v. 7, n. 2, p. 238-241, 2001. -
APA
Domenice, S., Nishi, M. Y., Billerbeck, A. E. C., Carvalho, F. M., Frade, E. M. C., Latronico, A. C., et al. (2001). Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue. Medical Science Monitor, 7( 2), 238-241. -
NLM
Domenice S, Nishi MY, Billerbeck AEC, Carvalho FM, Frade EMC, Latronico AC, Arnhold IJP, Mendonça BB. Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue. Medical Science Monitor. 2001 ; 7( 2): 238-241. -
Vancouver
Domenice S, Nishi MY, Billerbeck AEC, Carvalho FM, Frade EMC, Latronico AC, Arnhold IJP, Mendonça BB. Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue. Medical Science Monitor. 2001 ; 7( 2): 238-241. - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
- Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitibity syndrome in a brazilian cohort: five novel mutations in the androgen receptor gene
- 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
- An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis
- 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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