Meghan M DeBenedictis
8PUBLICATIONS
8CO-AUTHORS
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Publications (8)
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|Mar 02, 2023
A novel ocular phenotype associated with pathogenic variants in MFSD8 leading to macular dystrophy.Madeline Beckman, Leanne Clevenger, Meghan J DeBenedictis
|Apr 07, 2022
Severe retinal complications in Knobloch Syndrome - Three siblings without clinically apparent occipital defects and a review of the literature.Sruthi Arepalli, Meghan M DeBenedictis, Alex Yuan
|Dec 06, 2021
TULP1 related retinal dystrophy: report of rare and novel variants with a previously undescribed phenotype in two cases.H Al-Hindi, M Z Chauhan, R Sanders
|Aug 19, 2020
Inherited retinal degeneration current genetics practices - a needs assessment.Sydney Strait, Rebecca Loman, Lindsay Erickson
|Jul 28, 2020
A novel TIMP3 mutation associated with a retinitis pigmentosa-like phenotype.Meghan J DeBenedictis, Yosef Gindzin, Enrico Glaab
|Mar 27, 2020
Investigation of CEP290 genotype-phenotype correlations in a patient with retinitis pigmentosa, infertility, end-stage renal disease, and a novel mutation.Madeline Williamson, Elias Traboulsi, Meghan DeBenedictis
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