Deletion-mapping of chromosome 17 in patients with sporadic adrenocortical tumors associated with the Arg337His of the tumor suppreddor p53 (2003)
- Authors:
- USP affiliated authors: MENDONCA, BERENICE BILHARINHO DE - FM ; XAVIER, ANA CLAUDIA LATRONICO - FM
- Unidades: FM; FM
- Subjects: ENDOCRINOLOGIA; GENES
- Language: Inglês
- Imprenta:
- Place of publication: Philadelphia
- Date published: 2003
- Source:
- Título do periódico: Resumos
- Conference title: ENDO - The Endocrine Society's Annual Meeting
-
ABNT
PINTO, Emília M.; BILLERBECK, Ana Elisa; MENDONÇA, Berenice B.; LATRONICO, Ana Claudia. Deletion-mapping of chromosome 17 in patients with sporadic adrenocortical tumors associated with the Arg337His of the tumor suppreddor p53. Anais.. Philadelphia: [s.n.], 2003. -
APA
Pinto, E. M., Billerbeck, A. E., Mendonça, B. B., & Latronico, A. C. (2003). Deletion-mapping of chromosome 17 in patients with sporadic adrenocortical tumors associated with the Arg337His of the tumor suppreddor p53. In Resumos. Philadelphia. -
NLM
Pinto EM, Billerbeck AE, Mendonça BB, Latronico AC. Deletion-mapping of chromosome 17 in patients with sporadic adrenocortical tumors associated with the Arg337His of the tumor suppreddor p53. Resumos. 2003 ; -
Vancouver
Pinto EM, Billerbeck AE, Mendonça BB, Latronico AC. Deletion-mapping of chromosome 17 in patients with sporadic adrenocortical tumors associated with the Arg337His of the tumor suppreddor p53. Resumos. 2003 ; - 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
- 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
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
