Dr. Robert J Hopkin M.D.
Geneticist | Clinical Genetics (M.D.)
3333 Burnet Ave Ml 4006 Cincinnati OH, 45229About
Dr. Robert Hopkin practices Genetic Medicine in Cincinnati, OH. As a geneticist, Dr. Hopkin 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. Hopkin carries out studies, tests, and counsels patients with genetic diseases.
Education and Training
Univ of Nv Sch of Med, Reno Nv 1990
University Of Nevada School Of Medicine 1990
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- The trapped penis is a condition in which scarring at the distal prepuce forms a contracture that binds down the shaft of the penis.
- Prader Willi and Angelman syndromes: exemplars of genomic imprinting.
- Case of complex craniofacial anomalies, bilateral nasal proboscides, palatal pituitary, upper limbs reduction, and amnion rupture sequence: disorganization phenotype?
- Breast cancer genetics education for college women: an evaluation of approaches.
- Unexpected survival in a case of prenatally diagnosed non-mosaic trisomy 22: Clinical report and review of the natural history.
- Long-term survival in a patient with del(18)(q12.2q21.1).
- Upper airway malformation associated with partial trisomy 11q.
- Enzyme therapy for lysosomal storage disease: principles, practice, and prospects.
- Biochemical diagnosis of Antley-Bixler syndrome by steroid analysis.
- Undetectable maternal serum uE3 and postnatal abnormal sterol and steroid metabolism in Antley-Bixler syndrome.
- Genetic red flags: clues to thinking genetically in primary care practice.
- Use of the term "Antley-Bixler syndrome": minimizing confusion.
- Comparison of health-related quality of life between heterozygous women with Fabry disease, a healthy control population, and patients with other chronic disease.
- A new case of de novo 11q duplication in a patient with normal development and intelligence and review of the literature.
- Genetic service providers' practices and attitudes regarding adolescent genetic testing for carrier status.
Clinical Trials
Treatments
- Heart Disease
- Learning Disabilities
- Birth Defects
- Congenital Heart Disease
- Malnutrition
- Cleft Palate
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