Construction of a cDNA library from microdissected guinea pig crista ampullarisWILCOX, E. R; FEX, J.Hearing research. 1994, Vol 73, Num 1, pp 65-66, issn 0378-5955Article

Construction of a cDNA library from microdissected guinea pig organ of CortiWILCOX, E. R; FEX, J.Hearing research. 1992, Vol 62, Num 1, pp 124-126, issn 0378-5955Article

Epidemiology of Van der Woude syndrome from mutational analyses in affected patients from PakistanMALIK, S; KAKAR, N; HASNAIN, S et al.Clinical genetics. 2010, Vol 78, Num 3, pp 247-256, issn 0009-9163, 10 p.Article

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3AIHUI WANG; YONG LIANG; FRIEDMAN, T. B et al.Science (Washington, D.C.). 1998, Vol 280, Num 5368, pp 1447-1451, issn 0036-8075Article

Distinctive audiometric profile associated with DFNB21 alleles of TECTANAZ, S; ALASTI, F; MOWJOODI, A et al.Journal of medical genetics. 2003, Vol 40, Num 5, pp 360-363, issn 0022-2593, 4 p.Article

A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2LALWANI, A. K; BRISTER, J. R; FEX, J et al.American journal of human genetics. 1994, Vol 55, Num 4, pp 685-694, issn 0002-9297Article

The molecular genetics of Usher syndromeAHMED, Z. M; RIAZUDDIN, S; RIAZUDDIN, S et al.RIAZUDDIN, S; RIAZUDDIN, S et al.Clinical genetics. 2003, Vol 63, Num 6, pp 431-444, issn 0009-9163, 14 p.Article

Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutationsDESTEFANO, A. L; CUPPLES, L. A; LALWANI, A. K et al.Human genetics. 1998, Vol 102, Num 5, pp 499-506, issn 0340-6717Article

The PAX3 gene is mapped to human chromosome 2 together with a highly informative CA dinucleotide repeatWILCOX, E. R; RIVOLTA, M. N; PLOPLIS, B et al.Human molecular genetics (Print). 1992, Vol 1, Num 3, issn 0964-6906, p. 215Article

Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunctionNAZ, S; GRIFFITH, A. J; RIAZUDDIN, S et al.Journal of medical genetics. 2004, Vol 41, Num 8, pp 591-595, issn 0022-2593, 5 p.Article

OTOF encodes multiple long and short isoforms: Genetic evidence that the long ones underlie recessive deafness DFNB9YASUNAGA, S; GRATI, M; CHARDENOUX, S et al.American journal of human genetics. 2000, Vol 67, Num 3, pp 591-600, issn 0002-9297Article

Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type I in two familiesLALWANI, A. K; BRISTER, J. R; FEX, J et al.American journal of human genetics. 1995, Vol 56, Num 1, pp 75-83, issn 0002-9297Article

Some aspects of the mechanism of complexation of red kidney bean α-amylase inhibitor and α-amylaseWILCOX, E. R; WHITAKER, J. R.Biochemistry (Easton). 1984, Vol 23, Num 8, pp 1783-1791, issn 0006-2960Article

A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p1603LESPERANCE, M. M; HALL, J. W; WILCOX, E. R et al.Human molecular genetics (Print). 1995, Vol 4, Num 10, pp 1967-1972, issn 0964-6906Article

A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locusJAIN, P. K; FUKUSHIMA, K; WAYNE, S et al.Human molecular genetics (Print). 1995, Vol 4, Num 12, pp 2391-2394, issn 0964-6906Article

Waardenburg syndrome (WS) type 1 is caused by defects at multiple loci, one of which is near ALPP on chronosome 2 : first report of the WS consortiumFARRER, L. A; GRUNDFAST, K. M; GREENBERG, J et al.American journal of human genetics. 1992, Vol 50, Num 5, pp 902-913, issn 0002-9297Article

A new strain of Bacillus thuringiensis with activity against coleopteran insectsHERRNSTADT, C; SOARES, G. G; WILCOX, E. R et al.Bio/technology (New York, N.Y. 1983). 1986, Vol 4, Num 4, pp 305-308, issn 0733-222XArticle

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessPARK, H.-J; SHAUKAT, S; RIAZUDDIN, S et al.Journal of medical genetics. 2003, Vol 40, Num 4, pp 242-248, issn 0022-2593, 7 p.Article

A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C geneJAIN, P. K; LALWANI, A. K; LI, X. C et al.Genomics (San Diego, Calif.). 1998, Vol 50, Num 2, pp 290-292, issn 0888-7543Article

Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2YONG LIANG; AIHUI WANG; JAIN, P. K et al.American journal of human genetics. 1998, Vol 62, Num 4, pp 904-915, issn 0002-9297Article

A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degenerationLALWANI, A. K; LINTHICUM, F. H; LUXFORD, W. M et al.Audiology & neuro-otology. 1997, Vol 2, Num 3, pp 139-154, issn 1420-3030Article

A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6O'NEILL, M. E; MARIETTA, J; NI, L et al.Human molecular genetics (Print). 1996, Vol 5, Num 6, pp 853-856, issn 0964-6906Article

Genotype-phenotype correlations in type 1 Waardenburg syndromeLALWANI, A. K; MHATRE, A. N; SAN AGUSTIN, T. B et al.The Laryngoscope. 1996, Vol 106, Num 7, pp 895-902, issn 0023-852XConference Paper

Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14qFUKUSHIMA, K; ARABANDI RAMESH; PAWAIN JAIN et al.Human molecular genetics (Print). 1995, Vol 4, Num 9, pp 1643-1648, issn 0964-6906Article

A new strain of Bacillus thuringiensis with activity against coleopteran insectsHERRNSTADT, C; SOARES, G. G; WILCOX, E. R et al.Bio/technology (New York, N.Y. 1983). 1986, Vol 4, Num 4, pp 305-308, issn 0733-222XArticle