Overview
Ria Garg is a Medical Genetics provider in Detroit, Michigan. Her top areas of expertise are Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia, Camptodactyly Syndrome Guadalajara Type 1, Camptodactyly Taurinuria, and Camptodactyly Syndrome Guadalajara Type 2.
Her clinical research consists of co-authoring 40 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- OTHER MEDICAID
- STATE MEDICAID
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
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Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Experienced
- 2q37 Deletion SyndromeDr. Garg isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Garg isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Garg isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Garg isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Acrodermatitis EnteropathicaDr. Garg isExperienced. Learn about Acrodermatitis Enteropathica.
- Acrorenal Mandibular SyndromeDr. Garg isExperienced. Learn about Acrorenal Mandibular Syndrome.