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Results: 3

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
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