Corinne R. Abernathy

NF1 mutation analysis using a combined heteroduplex/SSCP approach

D. J. Driscoll, M. Wallace, S. Rasmussen, 1997, Human mutation.

Analysis of CpG C‐to‐T mutations in neurofibromatosis type 1

D. J. Driscoll, F. Collins, M. Wallace, 1998, Human mutation.

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.

Two NF1 mutations: Frameshift in the GAP‐related domain, and loss of two codons toward the 3′ end of the gene

S. Colman, M. Wallace, C. Abernathy, 1994, Human mutation.

Constitutional and mosaic large NF1 gene deletions in neurofibromatosis type 1.

C. Schwartz, S. Colman, M. Wallace, 1998, Journal of medical genetics.