CS
Highly rated in
54
conditions
Highly rated in
54
conditions

Specialties:Pediatrics | Medical Genetics
Experience:62 Years
Accepts:New PatientsMedicare
About Dr. C R. Scott

C Scott is a Pediatrics specialist and a Medical Genetics doctor in Seattle, Washington. Dr. Scott has been practicing medicine for over 62 years and is highly rated in 54 conditions, according to our data. His top areas of expertise are Fabry Disease, Megalencephalic Leukoencephalopathy with Subcortical Cysts, Multiple Sulfatase Deficiency, and SRD5A3-CDG. He is board certified in Pediatric Medicine and Medical Genetics And Genomics and licensed to treat patients in Washington. Dr. Scott is currently accepting new patients.

His clinical research consists of co-authoring 1 peer reviewed article in the past 15 years.

Insurance

MediFind strives to display the most accurate insurance information for every doctor. If you do not see your insurance listed for Dr. C R. Scott it is best to call his office and ask if your insurance is accepted.

Accepts Medicare

Dr. C R. Scott accepts the following insurance:

  •  PacificSource
  •  Premera

Call to see if your plan is accepted.
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Locations
  1959 Ne Pacific St, Seattle, WA 98195, US
Background & Education
Graduate Institution
University Of Washington School Of Medicine, 1959
Specialties
Pediatrics
Medical Genetics
Licenses
Clinical Genetics in WA
Board Certifications
Pediatric Medicine
Medical Genetics And Genomics
Hospital Affiliations
University Of Washington Medical Ctr
Languages Spoken
English
Gender
Male
Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Doctors 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.


1 Total Publications

Journal: European journal of medical genetics
Published —March 06, 2007
Molecular analysis of Turkish Gaucher disease patients: identification of novel mutations in glucocerebrosidase (GBA) gene.

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