Overview
Vernon Sutton is a Pediatrics specialist and a Medical Genetics provider in Houston, Texas. Dr. Sutton and is rated as a Distinguished provider by MediFind in the treatment of Genital Dwarfism. His top areas of expertise are Osteogenesis Imperfecta, Genital Dwarfism, Robinow Syndrome, and 2q37 Deletion Syndrome. Dr. Sutton is currently accepting new patients.
His clinical research consists of co-authoring 172 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 9 articles in the study of Genital Dwarfism.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Community Health
- Friday Health
- Humana
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.
James Lupski is a Pediatrics specialist and a Medical Genetics provider in Houston, Texas. Dr. Lupski and is rated as an Elite provider by MediFind in the treatment of Genital Dwarfism. His top areas of expertise are Potocki-Lupski Syndrome, Hypotonia, Smith-Magenis Syndrome, and Microcephaly. Dr. Lupski is currently accepting new patients.
Chaya Murali is a Pediatrics specialist and a Medical Genetics provider in Houston, Texas. Dr. Murali and is rated as an Advanced provider by MediFind in the treatment of Genital Dwarfism. Her top areas of expertise are Hereditary Hyperekplexia, Osteogenesis Imperfecta, Deafness Craniofacial Syndrome, Retinopathy Pigmentary Mental Retardation, and Myringotomy. Dr. Murali is currently accepting new patients.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Distinguished
- 2q37 Deletion Syndrome
- Acromicric Dysplasia
- Genital Dwarfism
- Osteogenesis Imperfecta
- Robinow Syndrome
- X-Linked Creatine Deficiency
- Advanced
- Achalasia Microcephaly Syndrome
- Alpha Mannosidosis
- Aplasia Cutis Congenita
- Clouston Syndrome
- Ectodermal Dysplasias
- Focal or Multifocal Malformations in Neuronal Migration
- Experienced
- Achondroplasia
- Argininosuccinic Aciduria
- Autism Spectrum Disorder
- Brachydactyly Mononen Type
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Childhood Pancreatitis