About the Doctor
Dr. Robin D. Clark is a clinical geneticist in San Bernardino, California, affiliated with five hospitals, including Riverside Community Hospital and Loma Linda University Medical Center. She received her medical degree from the University of Arizona College of Medicine-Tucson and completed a residency in Pediatrics at Tower Health/St. Christopher’s Hospital for Children (1978–1980) and the University of Arizona (1980–1981), followed by a fellowship in Medical Genetics at Los Angeles County-Harbor-UCLA Medical Center (1981–1984). She has been in practice for more than 20 years. Dr. Clark specializes in clinical genetics and clinical cytogenetics, evaluating and ordering diagnostic testing for patients suspected of having genetic diseases, and providing education, counseling, and referrals. She accepts Aetna, Cigna, Blue Cross, United Healthcare, and other major insurance plans.
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Medical School: University of Arizona College of Medicine-Tucson
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Residency: Tower Health/St. Christopher’s Hospital for Children (Pediatrics, 1978–1980); University of Arizona (Pediatrics, 1980–1981)
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Fellowship: Los Angeles County-Harbor-UCLA Medical Center (Medical Genetics, 1981–1984)
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Years of Experience: 21+ years
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Practice Setting: Outpatient genetics clinic and multiple hospital affiliations
Education & Training
Medical School – University of Arizona College of Medicine-Tucson
Residency – Tower Health/St. Christopher’s Hospital for Children, Pediatrics (1978–1980)
Residency – University of Arizona, Pediatrics (1980–1981)
Fellowship/Additional Training – Los Angeles County-Harbor-UCLA Medical Center, Medical Genetics (1981–1984)
Medical Conditions Treated
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Congenital anomalies and birth defects
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Chromosomal disorders (Down syndrome, Turner syndrome, Klinefelter syndrome, etc.)
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Single-gene disorders (cystic fibrosis, muscular dystrophy, Huntington’s disease, sickle cell disease)
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Intellectual disability and developmental delay of genetic origin
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Autism spectrum disorders (genetic evaluation)
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Mitochondrial disorders
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Neurogenetic conditions
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Hereditary cancer syndromes (BRCA, Lynch syndrome, etc.)
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Metabolic disorders (phenylketonuria, Gaucher disease)
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Skeletal dysplasias (achondroplasia, osteogenesis imperfecta)
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Teratogen exposure and genetic counseling during pregnancy
Medical Procedures Performed
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Comprehensive genetic evaluation and physical examination (dysmorphology assessment)
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Chromosome analysis (karyotype, FISH, chromosomal microarray)
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Molecular genetic testing (single gene, panel, whole exome/genome sequencing)
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Prenatal genetic testing (amniocentesis, chorionic villus sampling – referral or direct)
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Carrier screening for recessive disorders
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Newborn screening result interpretation and follow-up
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Genetic counseling for hereditary conditions
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Coordination of multidisciplinary care for genetic syndromes
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Interpretation of genetic test results for patients and families
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Referral to specialty clinics (cardiology, neurology, developmental pediatrics)
Services Offered
Dr. Clark provides comprehensive clinical genetics services for individuals of all ages with suspected or confirmed genetic disorders. Her practice includes thorough physical examinations (dysmorphology), detailed family history analysis, and selection of appropriate genetic tests. She also offers interpretation of complex genetic results and provides education and counseling to patients and families about diagnosis, inheritance patterns, recurrence risks, and management options. Dr. Clark collaborates closely with pediatricians, neurologists, maternal-fetal medicine specialists, and other subspecialists to ensure coordinated care. Services are available for prenatal, pediatric, and adult populations, including those with hereditary cancer predisposition or neurodevelopmental conditions.
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Diagnostic genetic evaluation – Detailed medical and family history, physical exam with dysmorphology assessment, review of prior records and imaging
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Genetic testing – Chromosomal microarray, whole exome sequencing, single-gene testing, FISH, karyotype, targeted mutation analysis
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Prenatal genetics – Counseling and testing for advanced maternal age, abnormal ultrasound findings, family history of genetic disorders; coordination of amniocentesis/CVS
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Oncogenetics – Hereditary cancer risk assessment, genetic testing for BRCA, Lynch syndrome, etc., and referral for enhanced screening or preventive surgery
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Pediatric genetics – Evaluation of developmental delay, intellectual disability, autism, multiple congenital anomalies, failure to thrive, metabolic disorders
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Adult genetics – Diagnosis or confirmation of genetic conditions in adulthood, family planning counseling, management of adult-onset disorders (e.g., Huntington’s)
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Genetic counseling – Explanation of inheritance patterns (autosomal dominant, recessive, X-linked), recurrence risk calculation, psychosocial support, family planning options
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Interpretation of results – Clear explanation of positive, negative, and uncertain findings; recommendations for medical management and surveillance
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Coordination of care – Referrals to cardiology, endocrinology, neurology, developmental pediatrics, physical therapy, and other specialists
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Education and advocacy – Provision of patient-friendly resources, connection to support groups, assistance with insurance authorization for genetic testing
Accepted Insurances
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Aetna (EPO, HMO, Medicare, POS, PPO)
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Blue Cross Blue Shield of Michigan (HMO, Medicare, POS, PPO)
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Cigna (PPO)
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Elevance (EPO, HMO, Medicare, POS, PPO)
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Florida Blue (PPO)
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Inland Empire Health Plan (Medicaid)
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Molina (HMO, Medicare)
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Regence Health Plans (PPO)
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United Healthcare (HMO, Medicare, POS, PPO)
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Also accepts Medicaid
Practice Locations
Address: 250 E Caroline Street, Suite A, San Bernardino, CA 92408
Phone: (909) 651-1899
Hospital Affiliations
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Riverside Community Hospital – Riverside, CA
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Emanate Health Queen of The Valley Hospital – Covina, CA
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Loma Linda University Medical Center – Loma Linda, CA
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Parkview Community Hospital Medical Center – Riverside, CA
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Pomona Valley Hospital Medical Center – Pomona, CA



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