K. Roux

Exon 10b of the NF1 gene represented a mutational hotspot and harbors a recurrent missense mutation y489c associated with aberrant splicing

J. Vance, G. Mortier, T. Callens, 1999, Genetics in Medicine.

Chromosome 17 loss‐of‐heterozygosity studies in benign and malignant tumors in neurofibromatosis type 1

S. Colman, K. Roux, M. Wallace, 2000, Genes, chromosomes & cancer.

Elastin region deletions in Williams syndrome.

C. Williams, K. Roux, M. Wallace, 1999, Genetic testing.

Molecular alterations resulting from frameshift mutations in peripheral myelin protein 22: Implications for neuropathy severity

K. Roux, L. Notterpek, B. Fletcher, 2005, Journal of neuroscience research.

The temporospatial expression of peripheral myelin protein 22 at the developing blood‐nerve and blood‐brain barriers

K. Roux, L. Notterpek, K. Roux, 2004, The Journal of comparative neurology.