Authors: Alagramam, KN Murcia, CL Kwon, HY Pawlowski, KS Wright, CG Woychik, RP

Citation: Kn. Alagramam et al., The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene, NAT GENET, 27(1), 2001, pp. 99-102

Authors: Alagramam, KN Yuan, HJ Kuehn, MH Murcia, CL Wayne, S Srisailpathy, CRS Lowry, RB Knaus, R Van Laer, L Bernier, FP Schwartz, S Lee, C Morton, CC Mullins, RF Ramesh, A Van Camp, G Hageman, GS Woychik, RP Smith, RJH

Citation: Kn. Alagramam et al., Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F (vol 10, pg 1709, 2001), HUM MOL GEN, 10(22), 2001, pp. 2603-2603

Authors: Alagramam, KN Yuan, HJ Kuehn, MH Murcia, CL Wayne, S Srisailpathy, CRS Lowry, RB Knaus, R Van Laer, L Bernier, FP Schwartz, S Lee, C Morton, CC Mullins, RF Ramesh, A Van Camp, G Hagemen, GS Woychik, RP Smith, RJH

Citation: Kn. Alagramam et al., Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F, HUM MOL GEN, 10(16), 2001, pp. 1709-1718

Authors: Alagramam, KN Zahorsky-Reeves, J Wright, CG Pawlowski, KS Erway, LC Stubbs, L Woychik, RP

Citation: Kn. Alagramam et al., Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer, HEARING RES, 148(1-2), 2000, pp. 181-191

Authors: Alagramam, KN Kwon, HY Cacheiro, NLA Stubbs, L Wright, CG Erway, LC Woychik, RP

Citation: Kn. Alagramam et al., A new mouse insertional mutation that causes sensorineural deafness and vestibular defects, GENETICS, 152(4), 1999, pp. 1691-1699