Zeinab Fadaie
Nijmegen, GE 6525GA, Netherlands
Last Updated: 09/26/2026
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Found 9 publications
Identification of a Complex Allele in IMPG2 as a Cause of Adult-Onset Vitelliform Macular Dystrophy.
Identification of a Complex Allele in IMPG2 as a Cause of Adult-Onset Vitelliform Macular Dystrophy.
Journal: Investigative ophthalmology & visual science
Published: May 24, 2022
Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseases.
Journal: NPJ genomic medicine
Published: May 20, 2021
Long-read technologies identify a hidden inverted duplication in a family with choroideremia.
Journal: HGG advances
Published: April 22, 2021
The Impact of Modern Technologies on Molecular Diagnostic Success Rates, with a Focus on Inherited Retinal Dystrophy and Hearing Loss.
Journal: International journal of molecular sciences
Published: February 05, 2021
BBS1 branchpoint variant is associated with non-syndromic retinitis pigmentosa.
Journal: Journal of medical genetics
Published: December 01, 2020
The identification of a RNA splice variant in TULP1 in two siblings with early-onset photoreceptor dystrophy.
Journal: Molecular genetics & genomic medicine
Published: November 27, 2018
Identification and Analysis of Genes Associated with Inherited Retinal Diseases.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: October 17, 2018
Showing 1-9 of 9
Last Updated: 09/26/2026