Dr. David H. Viskochil MD
Geneticist | Clinical Genetics (M.D.)
100 N Medical Dr Salt Lake City UT, 84113Rating
5/5
About
Dr. David Viskochil practices Genetic Medicine in Salt Lake City, UT. As a geneticist, Dr. Viskochil performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Viskochil carries out studies, tests, and counsels patients with genetic diseases.
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Natural history of Wolf-Hirschhorn syndrome: experience with 15 cases.
- Neurofibromatosis type 1: A model condition for the study of the molecular basis of variable expressivity in human disorders.
- Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1.
- Status of the human malformation map: 2002.
- Malignant peripheral nerve sheath tumor: a comparison of grade, immunophenotype, and cell cycle/growth activation marker expression in sporadic and neurofibromatosis 1-related lesions.
- It takes two to tango: mast cell and Schwann cell interactions in neurofibromas.
- Elevated catecholamine metabolites in patients with Costello syndrome.
- Interstitial deletion 8q11.2-q13 with congenital anomalies of CHARGE association.
- Case-control study of the muscular compartments and osseous strength in neurofibromatosis type 1 using peripheral quantitative computed tomography.
- Fetus with interstitial del(5)(p13.1p14.2) diagnosed postnatally with Cornelia de Lange syndrome.
- Double inactivation of NF1 in tibial pseudarthrosis.
- Pathologic and molecular analysis in a family with rare mixed supravalvar aortic and pulmonic stenosis.
- Bone mineral density in children and adolescents with neurofibromatosis type 1.
- Neurofibromatosis type 1 is a genetic skeletal disorder.
- Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients.
Clinical Trials
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Practice At 100 N Medical Dr
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Nearby Providers
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Dr. Joanne M. Jeter M.D.2000 CIRCLE OF HOPE DR SALT LAKE CITY UT 84112![]()
John M Opitz Other100 N Medical Dr Salt Lake City UT 84113![]()
John C. Carey Other100 N Medical Dr Salt Lake City UT 84113![]()
Dr. Susan Ora Lewin M.D100 N Medical Dr Salt Lake City UT 84113![]()
Dr. Lorenzo Davide Botto M.D.Medical Genetics Univ Utah 50 North Medical Dr Salt Lake City UT 84132![]()
Nicola Longo Other295 S CHIPETA WAY SALT LAKE CITY UT 84108
Nearest Hospitals
UNIVERSITY HEALTH CARE/UNIV HOSPITALS AND CLINICSl
50 NORTH MEDICAL DRIVE SALT LAKE CITY UT 84132PRIMARY CHILDRENS HOSPITALl
100 NORTH MARIO CAPECCHI DRIVE SALT LAKE CITY UT 84113SHRINERS HOSPITALS FOR CHILDREN - S L Cl
FAIRFAX ROAD AT VIRGINIA STREET SALT LAKE CITY UT 84103