William J. Kimberling

Isolation of a gene encoding a novel member of the nuclear receptor superfamily from the critical region of Usher syndrome type IIa at 1q41.

W. Kimberling, M. Ma-Edmonds, M. D. Weston, 1998, Genomics.

Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B.

D. Corey, W. Kimberling, M. Ramakrishnan, 1996, Genomics.

Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa.

C. Cremers, W. Kimberling, R. Ramesar, 2000, American journal of human genetics.

CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.

J. W. Askew, W. Reardon, H. Kremer, 2002, American journal of human genetics.

Spectrum of mutations in USH2A in British patients with Usher syndrome type II.

A. Bird, S. Bhattacharya, W. Kimberling, 2001, Experimental eye research.