Louise C Wilson
3PUBLICATIONS
7CO-AUTHORS
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Publications (3)
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|Aug 22, 2025
Absence of Syndactyly Associated With the Common Apert FGFR2 S252W Mutation: A Clinical Report and Likely Molecular Explanation.Ramy Saad, Claire Lawn, Honor Gartland
|Jul 27, 2024
A Comparison of Structural Variant Calling from Short-Read and Nanopore-Based Whole-Genome Sequencing Using Optical Genome Mapping as a Benchmark.Yang Pei, Melanie Tanguy, Adam Giess
|Jul 21, 2021
Biallelic P4HTM variants associated with HIDEA syndrome and mitochondrial respiratory chain complex I deficiency.Eleanor Hay, Louise C Wilson, Bethan Hoskins
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