Experienced in Brachydactyly Type B
Experienced in Brachydactyly Type B
4701 Ogletown Stanton Road, HGCC Suite 1340, 
Newark, DE 

Overview

Nina Powell is a Pediatrics specialist and a Medical Genetics provider in Newark, Delaware. Dr. Powell is rated as an Experienced provider by MediFind in the treatment of Brachydactyly Type B. Her top areas of expertise are Microcephaly, Chromosome 13q Deletion, Increased Head Circumference, and Perlman Syndrome.

Her clinical research consists of co-authoring 12 peer reviewed articles. MediFind looks at clinical research from the past 15 years.

Graduate Institution
University Of West Indies
Residency
Albert Einstein Medical Center
Specialties
Pediatrics
Medical Genetics
Licenses
Clinical Genetics in DE
Fellowships
University of Pittsburgh Medical Center
Hospital Affiliations
Christiana Hospital
Languages Spoken
English
Gender
Female

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Accepted insurance plans:

Aetna
  • EPO
  • HMO
  • POS
  • PPO

Locations

Center for Medical Genomics Office HGCC MDC
4701 Ogletown Stanton Road, HGCC Suite 1340, Newark, DE 19713
Other Locations
Center for Medical Genomics Office Helen F Graham, Ste 2200
4701 Ogletown Stanton Road, Suite 2200, Newark, DE 19713
Nemours duPont Hospital for Children
1600 Rockland Road, Department Of Pediatric Genetics, Wilmington, DE 19803

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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Jing Jin is a Pediatrics specialist and an Ophthalmologist in Wilmington, Delaware. Dr. Jin is rated as an Advanced provider by MediFind in the treatment of Brachydactyly Type B. Her top areas of expertise are Strabismus, Retinopathy Pigmentary Mental Retardation, Astigmatism, Endoscopy, and Lithotripsy. Dr. Jin is currently accepting new patients.

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Hilary J. Vernon
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Languages Spoken:
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Dr. Hilary Vernon is a Professor of Genetic Medicine and pediatrics at the Johns Hopkins University School of Medicine. She is also an attending physician at Kennedy Krieger Institute. Hilary Vernon has expertise in treating inborn errors of metabolism and mitochondrial disorders. She is the director of the Mitochondrial Care Center at The Johns Hopkins Hospital and the Barth Syndrome Interdisciplinary Clinic at the Kennedy Krieger Institute. Her research interests include understanding intermediary metabolism in Barth syndrome and in disorders of branch chain amino acid metabolism. Dr. Vernon also co-directs the Department of Genetic Medicine Clinical Trials Unit, and is the principal investigator on multiple clinical trials for rare diseases. Dr. Vernon received her medical degree and doctorate from Rutgers University, New Brunswick, New Jersey. She completed residencies in genetics and pediatrics at The Johns Hopkins University, and a fellowship in clinical laboratory biochemical genetics at The Johns Hopkins University. Dr. Vernon was recognized with the 2010 Francis F. Schwentker Award for Excellence in Research at Johns Hopkins University and the 2011 James B. Sidbury Jr. Fellowship in Biochemical Genetics at Johns Hopkins University. Dr. Vernon is rated as a Distinguished provider by MediFind in the treatment of Brachydactyly Type B. Her top areas of expertise are Methylmalonic Acidemia, Propionic Acidemia, Infantile Neutropenia, Progressive External Ophthalmoplegia, and Gastrostomy.

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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