Thomas B. Friedman
Laboratory of Molecular Genetics
National Institute on Deafness and Other Communication Disorders
National Institutes of Health
5 Research Court
USA;
Name/email consistency: high
- Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes. Schultz, J.M., Bhatti, R., Madeo, A.C., Turriff, A., Muskett, J.A., Zalewski, C.K., King, K.A., Ahmed, Z.M., Riazuddin, S., Ahmad, N., Hussain, Z., Qasim, M., Kahn, S.N., Meltzer, M.R., Liu, X.Z., Munisamy, M., Ghosh, M., Rehm, H.L., Tsilou, E.T., Griffith, A.J., Zein, W.M., Brewer, C.C., Riazuddin, S., Friedman, T.B. J. Med. Genet. (2011)
- Human nonsyndromic sensorineural deafness. Friedman, T.B., Griffith, A.J. Annu. Rev. Genomics. Hum. Genet (2003)
- DFNB3, spectrum of MYO15A recessive mutant alleles and an emerging genotype-phenotype correlation. Friedman, T.B., Hinnant, J.T., Ghosh, M., Boger, E.T., Riazuddin, S., Lupski, J.R., Potocki, L., Wilcox, E.R. Adv. Otorhinolaryngol. (2002)
- DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15. Friedman, T.B., Hinnant, J.T., Fridell, R.A., Wilcox, E.R., Raphael, Y., Camper, S.A. Adv. Otorhinolaryngol. (2000)
- Unconventional myosins and the genetics of hearing loss. Friedman, T.B., Sellers, J.R., Avraham, K.B. Am. J. Med. Genet. (1999)
