Dr. Richard Gregory Boles MD
Geneticist | Clinical Genetics (M.D.)
4650 W Sunset Blvd Ms# 90 Los Angeles CA, 90027Rating
5/5
About
Dr. Richard Boles practices Genetic Medicine in Los Angeles, CA. As a geneticist, Dr. Boles 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. Boles carries out studies, tests, and counsels patients with genetic diseases.
Education and Training
Univ of Ca, Los Angeles, Ucla Sch of Med, Los Angeles Ca 1987
University of California 1987
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Cleft palate, ptosis, digital anomalies and mental retardation: a new syndrome or a distal arthrogryposis variant?
- Detection of mitochondrial DNA mutations by temporal temperature gradient gel electrophoresis.
- Mitochondrial disease and cyclic vomiting syndrome.
- Rapid detection of FGFR mutations in syndromic craniosynostosis by temporal temperature gradient gel electrophoresis.
- Brain phenylalanine concentration in the management of adults with phenylketonuria.
- Mitochondrial DNA depletion, near-fatal metabolic acidosis, and liver failure in
- LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development.
- Mitochondrial disorders: a potentially under-recognized etiology of infantile spasms.
- Very long-chain acyl-CoA dehydrogenase deficiency in an infant presenting with massive hepatomegaly.
- Quantification of mitochondrial DNA heteroplasmy by temporal temperature gradient gel electrophoresis.
- Maternal inheritance in cyclic vomiting syndrome with neuromuscular disease.
- A prolonged local anaesthetic in control of post-tonsillectomy pain.
- Infantile mitochondrial DNA depletion syndrome associated with methylmalonic aciduria and 3-methylcrotonyl-CoA and propionyl-CoA carboxylase deficiencies in two unrelated patients: a new phenotype of mtDNA depletion syndrome.
- Severe reversible cardiomyopathy in four unrelated infants associated with mitochondrial DNA D-loop heteroplasmy.
- A case of rhinosporidiosis.
Dr. Richard Gregory Boles MD's Practice location
Practice At 4650 W Sunset Blvd Ms# 90
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