S. Dew-Knight

Haplotype analysis in Icelandic families defines a minimal interval for the macular corneal dystrophy type I gene.

M. Pericak-Vance, J. Baldwin, J. Vance, 1998, American journal of human genetics.

The gene encoding ganglioside- induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease

J. Gilbert, M. Pericak-Vance, J. Vance, 2001 .

Cloning and structural analysis of the human c-kit gene.

C. Decastro, R. Kaufman, G. R. Vandenbark, 1992, Oncogene.

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21

J. Gilbert, M. Pericak-Vance, J. Vance, 2002, Nature Genetics.

Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in Iceland.

J. Gilbert, J. Vance, F. Jónasson, 2000, Molecular vision.

Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genes.

J. Gilbert, J. Vance, F. Jónasson, 2000, Molecular vision.

Negative Regulation of DNA Replication by the Retinoblastoma Protein Is Mediated by Its Association with MCM7

S. Kornbluth, J. Horowitz, C. Musahl, 1998, Molecular and Cellular Biology.