Welcome to the Department of Pediatrics - Section of Genetics
Genetics provides comprehensive diagnostic evaluation for infants, children, adolescents and family members who have, or are suspected of having, disorders of genetic, congenital, hereditary or familial origins, including birth defects, syndromes of multiple malformations, inborn errors of metabolism, or familial cancer. Cytogenetic, DNA (gene), and special biochemical testing are arranged, as necessary, after appropriate genetic counseling. Teratogen information service is available as well. Testing for specific genetic disorders can be performed by our Genetics laboratory. Amino or organic acid analysis can be performed by our Biochem laboratory.
Our Mission:
- To discover new knowledge about the genetic determinants of human disease through laboratory, clinical and interdisciplinary research;
- To educate and mentor students, trainees, other interested health professionals and the public in the science, art and medical application of genetics;
- To apply genetics clinically to improve the health of patients, families, communities and the population; and
- To offer state-of-the-art genetic laboratory services for patients, family members and professional colleagues.
Clinical Services
Providing excellent patient care to children and adults with genetic conditions
Clinical Laboratory Services
Comprehensive services in cytogenetic and molecular studies, including congenital disorders, prenatal diagnosis, and hematologic/oncology disorders
Education & Training
Educating future leaders in the field of genetics
Research
Leading the way to cutting edge advances in genetics
Departmental Directory
Learn more about our diverse group of educators, clinical providers, and researchers