Below is a sampling of clinical trials and clinical research protocols from the Genetics & Genomics Research program and the Clinical Genetics program. For recent research findings, see our highlighted abstracts presented at the American Society of Human Genetics (ASHG) meeting.
Congenital heart disease
(see also Noonan syndrome)
Fragile X syndrome
Lysosomal storage disorders
- Genotype/Phenotype Correlation Study for Noonan Syndrome and related phenotypes (Coordinator: Erica Tworog-Dube, M.S., G.C., 617-525-4490)