Residents and medical students will learn to provide diagnostic evaluation, education, counseling and medical care for children and families with genetic disorders, birth defects, intellectual disabilities, developmental delays, neurological disorders, inborn errors of metabolism and chromosomal abnormalities.
Our division conducts 10 weekly clinics. Diagnostic procedures include:
- Metabolic studies
- Chromosome laboratory evaluations
- Peripheral blood and skin fibroblast chromosome evaluations
- Molecular genetic studies
- Genotype/phenotype correlation
Assistant Professor
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