Molecular autopsy reveals clues for genetic basis of congenital valve defect

Author(s):Show less -

Madia, F. A. R. ; Dias, A. T. ; Zanardo, E. A. ; Damasceno, J. G. ; Nascimento, A. M. ; Costa, T. V. M. M. ; Chehimi, S. N. ; Novo-Filho, G. M. ; Montenegro, M. M. ; Oliveira, Y. G. ; Freitas, A. B. ; Vieira, L. L. ; Schultz, R. ; Goncalves, F. T. ; Fridman, C. ; Kim, C. A. ; Kulikowski, L. D.

• Document type: Journal article
• Source: European Journal of Human Genetics; v. 27, p. 2-pg., 2019-07-01.
• FAPESP's process: 09/53105-9 - Application of molecular cytogenetic in the diagnosis of patients with congenital anomalies for the reduction of infant mortality
• Grantee: Leslie Domenici Kulikowski
• Support Opportunities: Research Grants - Research in Public Policies for the National Health Care System (PP-SUS)