Dr. Elizabeth K Schorry M.D.
Geneticist | Clinical Genetics (M.D.)
3333 Burnet Ave Ml 4006 Cincinnati OH, 45229About
Elizabeth Schorry, MD, received her undergraduate degree at the University of Cincinnati and her MD at the University of Michigan in Ann Arbor, Michigan. Dr. Schorry provides medical management, genetic ...
Education and Training
Univ of Mi Med Sch, Ann Arbor Mi 1982
University of Michigan Medical School 1982
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Social and emotional problems in children with neurofibromatosis type 1: evidence and proposed interventions.
- Neurofibromatosis in children: the role of the orthopaedist.
- A girl with partial trisomy 12q24.31 inherited from her father and a possible novel syndrome transmitted from her mother.
- Neurofibromatosis update.
- Gene symbol: COL1A2. Disease: osteogenesis imperfecta type II.
- The immature spine in type-1 neurofibromatosis.
- Gene expression analysis identifies potential biomarkers of neurofibromatosis type 1 including adrenomedullin.
- Variable expression of neurofibromatosis 1 in monozygotic twins.
- Fractures in children with neurofibromatosis type 1 from two NF clinics.
- Patient-reported outcomes in neurofibromatosis and schwannomatosis clinical trials.
- A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene.
- The Use of Magnetic Resonance Imaging Screening for Optic Pathway Gliomas in Children with Neurofibromatosis Type 1.
- Analysis of copy number variants in 11 pairs of monozygotic twins with neurofibromatosis type 1.
- Familial partial duplication (1)(p21p31).
Clinical Trials
Treatments
- Learning Disabilities
- Birth Defects
- Pain
Fellowships
- Genetics, Children's Hospital Medical Center, Cincinnati, OH 1985
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