Investigation of submicroscopic genomic alterations by array CGH in specific phenotypes: non-syndromic hereditary deafness and defects of Müllerian development

• Grant number: 09/05620-1
• Support type: Scholarships in Brazil - Post-Doctorate
• Effective date (Start): July 01, 2009
• Effective date (End): June 30, 2013
• Field of knowledge: Biological Sciences - Genetics - Human and Medical Genetics
• Principal Investigator: Carla Rosenberg
• Grantee: Erika Cristina Lopes Burrone de Freitas
• Home Institution: Instituto de Biociências (IB). Universidade de São Paulo (USP). São Paulo , SP, Brazil
• Associated research grant: 09/00898-1 - Submicroscopic genomic imbalances associated with specific congenital abnormalities and mental deficiency phenotypes, AP.TEM

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)

DANTAS, VITOR G. L.; FREITAS, ERIKA L.; DELLA-ROSA, VALTER A.; LEZIROVITZ, KARINA; DE MORAES, ANA MARIA S. M.; RAMOS, SILVIA B.; OITICICA, JEANNE; ALVES, LEANDRO U.; PEARSON, PETER L.; ROSENBERG, CARLA; MINGRONI-NETTO, REGINA C. Novel partial duplication of EYA1 causes branchiootic syndrome in a large Brazilian family. INTERNATIONAL JOURNAL OF AUDIOLOGY, v. 54, n. 9, p. 593-598, 2015. Web of Science Citations: 1.