Tracy A. Fletcher
St Mary's Hospital
Manchester, ENG, United Kingdom
Manchester, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 8 publications
Long-Read Nanopore Sequencing of RPGR ORF15 is Enhanced Following DNase I Treatment of MinION Flow Cells.
Journal: Molecular diagnosis & therapy
Published: May 18, 2023
EyeG2P: an automated variant filtering approach improves efficiency of diagnostic genomic testing for inherited ophthalmic disorders.
Journal: Journal of medical genetics
Published: May 07, 2022
Correction: Clinical utility of genetic testing in 201 preschool children with inherited eye disorders.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 23, 2020
Clinical utility of genetic testing in 201 preschool children with inherited eye disorders.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 23, 2019
Clinical and genetic variability in children with partial albinism.
Journal: Scientific reports
Published: June 13, 2019
Diagnostic yield of panel-based genetic testing in syndromic inherited retinal disease.
Journal: European journal of human genetics : EJHG
Published: May 30, 2019
Severe retinal degeneration in women with a c.2543del mutation in ORF15 of the RPGR gene.
Journal: Molecular vision
Published: July 06, 2014
A clinical molecular genetic service for United Kingdom families with choroideraemia.
Journal: European journal of medical genetics
Published: November 04, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026