Physician
Medical Genetics
Dr. Kerry B. Jedele, MD
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Kerry Jedele practices Medical Genetics. She studied medicine at University of Wisconsin School of Medicine and Public Health. She has 1 awards "Fellow (FAAP)". Kerry Jedele has written publications. She has 17 publications published with PubMed. The lastest paper is: 'A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutation...'
Publications
- Compound heterozygosity for MSH6 mutations in a pediatric lymphoma patient.
- The overlapping spectrum of rett and angelman syndromes: a clinical review.
- MRX42: two linkage intervals, one in the pericentromeric region and one in Xq26, and the impact for carrier risk estimation.
- Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3).
- Nonsyndromic X-linked mental retardation: mapping of MRX58 to the pericentromeric region.
- UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1-...
- A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutation...
- Spinal and bulbar muscular atrophy (SBMA): somatic stability of an expanded CAG repeat in fetal tissues.
- Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 unique mutations without correlation to clinical course.
- Large intergenerational variation in age of onset in two young patients with Huntington's disease presenting as dyskinesia.
- Discordant monozygotic twins with the Schimmelpenning-Feuerstein-Mims syndrome.
- FRAXE testing.
- Velo-cardio-facial syndrome associated with ventricular septal defect, pulmonary atresia, and hypoplastic pulmonary arteries.
- Linkage of nonspecific X-linked mental retardation to Xq21.31.
- Familial dermographism.
- Frequency of congenital heart defects in patients with hemophilia.
Schools
University Of Wisconsin Medical School
Mayo Clinic Rochester
Doctors Specialties
- Pediatrics
- Medical Genetics
Accepted Insurances
Awards
- Fellow (FAAP)
Education
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Mayo School of Graduate Medical Education -
University of Wisconsin School of Medicine and Public Health
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