Wilcox ER - Search Results

1

The PAX3 gene is mapped to human chromosome 2 together with a highly informative CA dinucleotide repeat.

Wilcox ER, Rivolta MN, Ploplis B, Potterf SB, Fex J. Wilcox ER, et al. Hum Mol Genet. 1992 Jun;1(3):215. doi: 10.1093/hmg/1.3.215-a. Hum Mol Genet. 1992. PMID: 1303187 No abstract available.

2

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 families.

Lalwani AK, Brister JR, Fex J, Grundfast KM, Ploplis B, San Agustin TB, Wilcox ER. Lalwani AK, et al. Among authors: wilcox er. Am J Hum Genet. 1995 Jan;56(1):75-83. Am J Hum Genet. 1995. PMID: 7825605 Free PMC article.

3

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

Lalwani AK, Brister JR, Fex J, Grundfast KM, Pikus AT, Ploplis B, San Agustin T, Skarka H, Wilcox ER. Lalwani AK, et al. Among authors: wilcox er. Am J Hum Genet. 1994 Oct;55(4):685-94. Am J Hum Genet. 1994. PMID: 7942846 Free PMC article.

4

G protein Gi2 alpha in the cochlea: cloning and selective occurrence in receptor cells.

Tachibana M, Asano T, Wilcox E, Yokotani N, Rivolta MN, Fex J. Tachibana M, et al. Brain Res Mol Brain Res. 1994 Feb;21(3-4):355-8. doi: 10.1016/0169-328x(94)90267-4. Brain Res Mol Brain Res. 1994. PMID: 8170357

5

Construction of a cDNA library from microdissected guinea pig organ of Corti.

Wilcox ER, Fex J. Wilcox ER, et al. Hear Res. 1992 Sep;62(1):124-6. doi: 10.1016/0378-5955(92)90208-5. Hear Res. 1992. PMID: 1358871

6

A novel and simple methodology to generate subtracted cDNA libraries.

Rivolta MN, Wilcox ER. Rivolta MN, et al. Among authors: wilcox er. Nucleic Acids Res. 1995 Jul 11;23(13):2565-6. doi: 10.1093/nar/23.13.2565. Nucleic Acids Res. 1995. PMID: 7630738 Free PMC article. No abstract available.

7

Construction of a cDNA library from microdissected guinea pig crista ampullaris.

Wilcox ER, Fex J. Wilcox ER, et al. Hear Res. 1994 Feb;73(1):65-6. doi: 10.1016/0378-5955(94)90283-6. Hear Res. 1994. PMID: 8157507

8

A novel zinc finger gene preferentially expressed in the retina and the organ of Corti localizes to human chromosome 12q24.3.

Rivolta MN, Negrini C, Wilcox ER. Rivolta MN, et al. Among authors: wilcox er. Biochim Biophys Acta. 1996 May 2;1306(2-3):127-32. doi: 10.1016/0167-4781(96)00022-x. Biochim Biophys Acta. 1996. PMID: 8634327

9

Selective amplification and partial sequencing of cDNAs encoding G protein alpha subunits from cochlear tissues.

Tachibana M, Wilcox E, Yokotani N, Schneider M, Fex J. Tachibana M, et al. Hear Res. 1992 Sep;62(1):82-8. doi: 10.1016/0378-5955(92)90204-z. Hear Res. 1992. PMID: 1429253

10

Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan.

Ahmed ZM, Li XC, Powell SD, Riazuddin S, Young TL, Ramzan K, Ahmad Z, Luscombe S, Dhillon K, MacLaren L, Ploplis B, Shotland LI, Ives E, Riazuddin S, Friedman TB, Morell RJ, Wilcox ER. Ahmed ZM, et al. Among authors: wilcox er. BMC Med Genet. 2004 Sep 24;5:24. doi: 10.1186/1471-2350-5-24. BMC Med Genet. 2004. PMID: 15447792 Free PMC article.

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