Valerie Slegesky, MS
Instructor, Pediatrics-Clinical Genetics and Metabolism
Guo, H, et al (2020). NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism. American Journal of Human Genetics 107(5): 963-976.
Legro, N, et al (2020). Novel FAM177A1 variants cause macrocephaly, developmental delay, and intellectual disability in 8 individuals. Presented at the annual meeting of the American College of Medical Genetics (March 2020, virtual).
National Society of Genetic Counselors, Member
- Clinical Genetics and Genomics (MD)