Clinical Molecular Genetics Fellowship
The Molecular Diagnostic Laboratory at UNC provides experience with tests including cystic fibrosis, fragile X mental retardation, hemochromatosis, factor V Leiden and prothrombin, a1-antitrypsin deficiency, MERRF and MELAS, connexin mutations, hereditary cancers, EBV viral load, and chromosomal breakpoints in leukemias, as well as monitoring of bone marrow transplants with polymorphic microsatellite markers. State-of-the-art technologies and instrumentation are used in all of these tests, and the laboratory has a strong research foundation. Our postdoctoral training programs in medical genetics are provided by collaboration among individuals from numerous academic units including Anatomy & Cell Biology, Biochemistry, Genetics, Medicine, Obstetrics & Gynecology, Pathology & Laboratory Medicine, Pediatrics, the Curriculum in Genetics and Molecular Biology, the School of Public Health, the Cancer Center, the Center for Genomics, the Neuroscience Center, the Gene Therapy Center, and the Birth Defects Center. The University of North Carolina Hospitals, with a statewide referral base, provide a rich source for clinical experience in all subspecialty areas. Our medical genetics programs have been a focus for statewide referrals since 1970. Program Requirements: Ph.D. in an area related to genetics or M.D. required. Physicians are also eligible for fellowship training in Molecular Genetic Pathology. Stipends: Fellowship stipends are based on the trainee's number of years of postdoctoral training. Program Director: Jessica Booker, PhD Faculty Members: Applications: Send a cover letter, curriculum vitae, and the names of three references by December 1 to… Jessica Booker, PhD Telephone: 919-966-7894
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