T. Smith

A PAX3 polymorphism (T315K) in a family exhibiting Waardenburg Syndrome type 2.

A. Lalwani, E. Wilcox, C. Wang, 1998, Molecular and cellular probes.

A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene.

A. Lalwani, I. Verma, E. Wilcox, 1998, Genomics.

OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9.

C. Petit, S. Chardenoux, T. Friedman, 2000, American journal of human genetics.