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

• Grant number: 11/02865-3
• Support Opportunities: 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 Investigator: Maricilda Palandi de Mello
• Grantee: Helena Fabbri Scallet
• Host Institution: Centro de Biologia Molecular e Engenharia Genética (CBMEG). Universidade Estadual de Campinas (UNICAMP). Campinas , SP, Brazil

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. (09/08320-9, 08/01964-5, 08/03168-1, 11/02865-3)

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. (11/02865-3)

Academic Publications

(References retrieved automatically from State of São Paulo Research Institutions)

SCALLET, Helena Fabbri. NR5A1 molecular analysis in 46,XY patients with disorders of sex development. 2013. Master's Dissertation - Universidade Estadual de Campinas (UNICAMP). Instituto de Biologia Campinas, SP.