Authors:
Lin, D
Goldstein, JA
Mhatre, AN
Lustig, LR
Pfister, M
Lalwani, AK
Citation: D. Lin et al., Assessment of denaturing high-performance liquid chromatography (DHPLC) inscreening for mutations in connexin 26 (GJB2), HUM MUTAT, 18(1), 2001, pp. 42-51
Authors:
Kho, ST
Pettis, RM
Mhatre, AN
Lalwani, AK
Citation: St. Kho et al., Safety of adeno-associated virus as cochlear gene transfer vector: Analysis of distant spread beyond injected cochleae, MOL THER, 2(4), 2000, pp. 368-373
Authors:
Riazuddin, S
Castelein, CM
Ahmed, ZM
Lalwani, AK
Mastroianni, MA
Naz, S
Smith, TN
Liburd, NA
Friedman, TB
Griffith, AJ
Riazuddin, S
Wilcox, ER
Citation: S. Riazuddin et al., Dominant modifier DFNM1 suppresses recessive deafness DFNB26, NAT GENET, 26(4), 2000, pp. 431-434
Citation: Cj. Tseng et Ak. Lalwani, Cracking the auditory genetic code: Part II. Syndromic hereditary hearing impairment, AM J OTOL, 21(3), 2000, pp. 437-451
Citation: J. Johnson et Ak. Lalwani, Sensorineural and conductive hearing loss associated with lateral semicircular canal malformation, LARYNGOSCOP, 110(10), 2000, pp. 1673-1679
Authors:
Lalwani, AK
Goldstein, JA
Kelley, MJ
Luxford, W
Castelein, CM
Mhatre, AN
Citation: Ak. Lalwani et al., Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9, AM J HU GEN, 67(5), 2000, pp. 1121-1128
Authors:
Yasunaga, S
Grati, M
Chardenoux, S
Smith, TN
Friedman, TB
Lalwani, AK
Wilcox, ER
Petit, C
Citation: S. Yasunaga et al., OTOF encodes multiple long and short isoforms: Genetic evidence that the long ones underlie recessive deafness DFNB9, AM J HU GEN, 67(3), 2000, pp. 591-600
Authors:
Han, JJ
Mhatre, AN
Wareing, M
Pettis, R
Gao, WQ
Zufferey, RN
Trono, D
Lalwani, AK
Citation: Jj. Han et al., Transgene expression in the guinea pig cochlea mediated by a lentivirus-derived gene transfer vector, HUM GENE TH, 10(11), 1999, pp. 1867-1873