Whole Exome Sequencing in Brazilian individuals with intellectual disability, Neurodevelopmental Delay and (or) Multiple Congenital Anomalies with Copy Number Variants of Uncertain Clinical Significance detected by Chromosomal Microarray Analysis

Author(s):Show less -

Spineli-Silva, S. ; de Leeuw, N. ; dos Santos, A. P. ; Leijsten, N. ; Ruiterkamp-Versteeg, M. H. A. ; Prota, J. R. M. ; Maciel-Guerra, A. T. ; Marques-de-Faria, A. ; Steiner, C. E. ; Gil-da-Silva-Lopes, V. L. ; Vieira, T. P.

• Document type: Journal article
• Source: European Journal of Human Genetics; v. 28, n. SUPPL 1, p. 1-pg., 2020-12-01.
• FAPESP's process: 18/08890-9 - Detection and consequences of imbalances in the human genome
• Grantee: Társis Antônio Paiva Vieira
• Support Opportunities: Regular Research Grants