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NR5A1 molecular analysis in 46,XY patients with sex development disorders

Grant number: 11/02865-3
Support type:Scholarships in Brazil - Master
Effective date (Start): August 01, 2011
Effective date (End): February 28, 2013
Field of knowledge:Health Sciences - Medicine - Medical Clinics
Principal researcher:Maricilda Palandi de Mello
Grantee:Helena Fabbri Scallet
Home Institution: Centro de Biologia Molecular e Engenharia Genética (CBMEG). Universidade Estadual de Campinas (UNICAMP). Campinas , SP, Brazil
News published in Agência FAPESP Newsletter about the scholarship:
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Scientific publications
(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
FABBRI, HELENA CAMPOS; RIBEIRO DE ANDRADE, JULIANA GABRIEL; SOARDI, FERNANDA CAROLINE; DE CALAIS, FLAVIA LEME; PETROLI, REGINALDO JOSE; MACIEL-GUERRA, ANDREA TREVAS; GUERRA-JUNIOR, GIL; DE MELLO, MARICILDA PALANDI. The novel p.Cys65Tyr mutation in NR5A1 gene in three 46,XY siblings with normal testosterone levels and their mother with primary ovarian insufficiency. BMC MEDICAL GENETICS, v. 15, JAN 10 2014. Web of Science Citations: 17.
RIBEIRO DE ANDRADE, JULIANA GABRIEL; MARQUES-DE-FARIA, ANTONIA PAULA; FABBRI, HELENA CAMPOS; DE MELLO, MARICILDA PALANDI; GUERRA-JUNIOR, GIL; MACIEL-GUERRA, ANDREA TREVAS. Long-Term Follow-Up of Patients with 46, XY Partial Gonadal Dysgenesis Reared as Males. INTERNATIONAL JOURNAL OF ENDOCRINOLOGY, 2014. Web of Science Citations: 7.

Please report errors in scientific publications list by writing to: cdi@fapesp.br.