Publications by authors named "Eloise J Prijoles"

10Publications

Filling in the gaps on FILS syndrome: A case report and literature review.

Pediatr Dermatol 2020 Sep 23;37(5):915-917. Epub 2020 Jul 23.

Department of Dermatology and Dermatologic Surgery, Medical University of South Carolina, Charleston, SC, USA.

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http://dx.doi.org/10.1111/pde.14274DOI Listing
September 2020

Assessing the barriers to cardiac care in carriers of Duchenne and Becker muscular dystrophy.

J Genet Couns 2019 10 1;28(5):993-1002. Epub 2019 Aug 1.

Greenwood Genetic Center, Greenwood, South Carolina.

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http://dx.doi.org/10.1002/jgc4.1151DOI Listing
October 2019

Williams-Beuren syndrome in diverse populations.

Am J Med Genet A 2018 05;176(5):1128-1136

Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland.

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http://doi.wiley.com/10.1002/ajmg.a.38672
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http://dx.doi.org/10.1002/ajmg.a.38672DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007881PMC
May 2018

Mowat-Wilson syndrome with associated dysphagia.

Am J Med Genet A 2010 Feb;152A(2):484-5

Division of Genetics, Department of Pediatrics, University of South Florida, Tampa, Florida 33606, USA.

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http://dx.doi.org/10.1002/ajmg.a.33211DOI Listing
February 2010