Authors:
Bikhazi, PH
Roeder, E
Attaie, A
Lalwani, AK
Citation: Ph. Bikhazi et al., Familial paragangliomas: The emerging impact of molecular genetics on evaluation and management, AM J OTOL, 20(5), 1999, pp. 639-643
Authors:
Lalwani, AK
Luxford, WM
Mhatre, AN
Attaie, A
Wilcox, ER
Castelein, CM
Citation: Ak. Lalwani et al., A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration, AM J HU GEN, 64(1), 1999, pp. 318-323
Authors:
Lalwani, AK
Attaie, A
Randolph, T
Deshmukh, D
Wang, C
Mhatre, A
Wilcox, E
Citation: Ak. Lalwani et al., Point mutation in the MITF gene causing Waardenburg syndrome type II in a three-generation Indian family, AM J MED G, 80(4), 1998, pp. 406-409