A novel and simple methodology to generate subtracted cDNA libraries.

Por Rivolta, M N, Wilcox, E R
Publicado em 1995

Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction

Por Naz, S, Griffith, A, Riazuddin, S, Hampton, L, Battey, J, Khan, S, Riazuddin, S, Wilcox, E, Friedman, T
Publicado em 2004

Distinctive audiometric profile associated with DFNB21 alleles of TECTA

Por Naz, S, Alasti, F, Mowjoodi, A, Riazuddin, S, Sanati, M, Friedman, T, Griffith, A, Wilcox, E, Riazuddin, S
Publicado em 2003

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

0450. Systemic dysregulation of the angiopoietin-1/2 system in adults undergoing cardiopulmonary bypass (CBP)

Por Charbonney, E, Wilcox, E, Shan, Y, d'Empaire, P Perez, Dugal, A, Glogauer, M, Rubenfeld, GD, Sutherland, S, Lilles, C, Dos Santos, C
Publicado no Intensive Care Med Exp (2014)

Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

Por Ben-Yosef, T., Wattenhofer, M., Riazuddin, S., Ahmed, Z., Scott, H., Kudoh, J., Shibuya, K., Antonarakis, S., Bonne-Tamir, B., Radhakrishna, U., Naz, S., Ahmed, Z., Riazuddin, S., Pandya, A., Nance, W., Wilcox, E., Friedman, T., Morell, R.
Publicado em 2001

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness

Por Park, H, Shaukat, S, Liu, X, Hahn, S, Naz, S, Ghosh, M, Kim, H, Moon, S, Abe, S, Tukamoto, K, Riazuddin, S, Kabra, M, Erdenetungalag, R, Radnaabazar, J, Khan, S, Pandya, A, Usami, S, Nance, W, Wilcox, E, Riazuddin, S, Griffith, A
Publicado em 2003

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