Mutation analysis and effects on the SRY gene expression in XY gonadal dysgenesis

(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)

CUNHA, J. L.; SOARDI, F. C.; BERNARDI, R. D.; OLIVEIRA, L. E. C.; BENEDETTI, C. E.; GUERRA-JUNIOR, G.; MACIEL-GUERRA, A. T.; DE MELLO, M. P.. The novel p.E89K mutation in the SRY gene inhibits DNA binding and causes the 46,XY disorder of sex development. Brazilian Journal of Medical and Biological Research, v. 44, n. 4, p. 361-365, APR 2011. (08/03168-1, 07/00900-0)

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

CUNHA JÚNIOR, José Luiz Rosenberis. SRY gene mutation analysis and functional effects in cases of XY gonadal dysgenesis. 2010. Master's Dissertation - Universidade Estadual de Campinas (UNICAMP). Instituto de Biologia Campinas, SP.