Scanning Electrochemical Microscopy as a Novel Proximity Sensor for Atraumatic Cochlear Implant Insertion

Por Watanabe, H., Velmurugan, J., Mirkin, M. V., Svirsky, M. A., Lalwani, A. K., Llinas, R. R.
Publicado em 2014

A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration.

Por Lalwani, A K, Luxford, W M, Mhatre, A N, Attaie, A, Wilcox, E R, Castelein, C M
Publicado em 1999

Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type 1 in two fam...

Por Lalwani, A K, Brister, J R, Fex, J, Grundfast, K M, Ploplis, B, San Agustin, T B, Wilcox, E R
Publicado em 1995

A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.

Por Lalwani, A. K., Brister, J. R., Fex, J., Grundfast, K. M., Pikus, A. T., Ploplis, B., San Agustin, T., Skarka, H., Wilcox, E. R.
Publicado em 1994

Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.

Por Liang, Y, Wang, A, Probst, F J, Arhya, I N, Barber, T D, Chen, K S, Deshmukh, D, Dolan, D F, Hinnant, J T, Carter, L E, Jain, P K, Lalwani, A K, Li, X C, Lupski, J R, Moeljopawiro, S, Morell, R, Negrini, C, Wilcox, E R, Winata, S, Camper, S A, Friedman, T B
Publicado em 1998