Genetic studies of midline facial defects with ocular hypertelorism

• Grant number: 05/03480-7
• Support Opportunities: Regular Research Grants
• Start date: May 01, 2006
• End date: July 31, 2008
• Field of knowledge: Biological Sciences - Genetics - Human and Medical Genetics
• Principal Investigator: Vera Lúcia Gil da Silva Lopes
• Grantee: Vera Lúcia Gil da Silva Lopes
• Host Institution: Faculdade de Ciências Médicas (FCM). 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)

FREITAS, ERIKA L.; GRIBBLE, SUSAN M.; SIMIONI, MILENA; VIEIRA, TARSIS P.; SILVA-GRECCO, ROSEANE L.; BALARIN, MARLY A. S.; PRIGMORE, ELENA; KREPISCHI-SANTOS, ANA C.; ROSENBERG, CARLA; SZUHAI, KAROLY; et al. Maternally Inherited Partial Monosomy 9p (pter -> p24.1) and Partial Trisomy 20p (pter -> p12.1) Characterized by Microarray Comparative Genomic Hybridization. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, v. 155A, n. 11, p. 2754-2761, NOV 2011. (05/03480-7)

SIMIONI, M.; FREITAS, E. LOPES; VIEIRA, T. PAIVA; LOPES-CENDES, I.; GIL-DA-SILVA-LOPES, V. LUCIA. Investigation of the 22q11.2 candidate region in patients with midline facial defects with hypertelorism. JOURNAL OF APPLIED GENETICS, v. 51, n. 2, p. 219-221, 2010. (05/03480-7)