Artigo de periodico

Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment (2007)

• Authors:
  • Coutinho, Debora C.
  • Mendonça, Berenice B.
  • Coletta, Rocio R. D.
  • Costa, Elaine M. F.
  • Pachi, Paulo R.
  • Boguszewski, Margaret C. S.
  • Damiani, Durval
  • Arnhold, Ivo J. P.
  • Jorge, Alexander A. L.
• USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM
• Unidades: FM
• DOI: 10.1210/jc.2007-1661
• Subjects: POLIMORFISMO; BIOLOGIA MOLECULAR; MUTAÇÃO GENÉTICA; NUCLEOTÍDEOS (ANÁLISE); CRESCIMENTO E DESENVOLVIMENTO (ESTUDO CLÍNICO)
• Language: Inglês
• Imprenta:
  • Place of publication: Philadelphia
  • Date published: 2007
• Source:
  • Título do periódico: Journal of Clinical Endocrinology and Metabolism
  • ISSN: 0021-972X
  • Volume/Número/Paginação/Ano: v. 92, n. 12, p. 4889-4892, 2007

Informações sobre o DOI: 10.1210/jc.2007-1661 (Fonte: oaDOI API)
• Este periódico é de assinatura
• Este artigo é de acesso aberto
• URL de acesso aberto
• Cor do Acesso Aberto: bronze

---

How to cite

A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

• ABNT

  COUTINHO, Debora C.; MENDONÇA, Berenice B.; COLETTA, Rocio R. D.; et al. Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment. Journal of Clinical Endocrinology and Metabolism, Philadelphia, v. 92, n. 12, p. 4889-4892, 2007. Disponível em: < http://dx.doi.org/10.1210/jc.2007-1661 > DOI: 10.1210/jc.2007-1661.

• APA

  Coutinho, D. C., Mendonça, B. B., Coletta, R. R. D., Costa, E. M. F., Pachi, P. R., Boguszewski, M. C. S., et al. (2007). Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment. Journal of Clinical Endocrinology and Metabolism, 92( 12), 4889-4892. doi:10.1210/jc.2007-1661

• NLM

  Coutinho DC, Mendonça BB, Coletta RRD, Costa EMF, Pachi PR, Boguszewski MCS, Damiani D, Arnhold IJP, Jorge AAL. Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment [Internet]. Journal of Clinical Endocrinology and Metabolism. 2007 ; 92( 12): 4889-4892.Available from: http://dx.doi.org/10.1210/jc.2007-1661

• Vancouver

  Coutinho DC, Mendonça BB, Coletta RRD, Costa EMF, Pachi PR, Boguszewski MCS, Damiani D, Arnhold IJP, Jorge AAL. Polymorphisms Identified in the Upstream Core Polyadenylation Signal of IGF1 Gene Exon 6 Do Not Cause Pre- and Postnatal Growth Impairment [Internet]. Journal of Clinical Endocrinology and Metabolism. 2007 ; 92( 12): 4889-4892.Available from: http://dx.doi.org/10.1210/jc.2007-1661

Últimas obras dos mesmos autores vinculados com a USP cadastradas na BDPI:

• 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