Experienced in Singleton-Merten Syndrome
Experienced in Singleton-Merten Syndrome
10 Center Drive Msc 1851, Bldg. 10, Room 10c-103, Nhgri, Nih, 
Bethesda, MD 

Overview

William Gahl is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Gahl is rated as an Experienced provider by MediFind in the treatment of Singleton-Merten Syndrome. His top areas of expertise are Oculocutaneous Albinism Type 2, Hermansky-Pudlak Syndrome, Oculocutaneous Albinism Type 1, Oculocutaneous Albinism, and Deep Brain Stimulation.

His clinical research consists of co-authoring 382 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Singleton-Merten Syndrome.

Specialties
Medical Genetics
Pediatrics
Licenses
Clinical Genetics in WI
Languages Spoken
English
Gender
Male

Insurance

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Locations

10 Center Drive Msc 1851, Bldg. 10, Room 10c-103, Nhgri, Nih, Bethesda, MD 20892

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.


378 Total Publications

Diffusion tensor imaging in Chediak Higashi Disease.
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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.

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