Brown KA - Search Results

1

Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1.

Brown KA, al-Gazali LI, Moynihan LM, Lench NJ, Markham AF, Mueller RF. Brown KA, et al. J Med Genet. 1997 Aug;34(8):685-7. doi: 10.1136/jmg.34.8.685. J Med Genet. 1997. PMID: 9279765 Free PMC article.

2

Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175.

Brown KA, Janjua AH, Karbani G, Parry G, Noble A, Crockford G, Bishop DT, Newton VE, Markham AF, Mueller RF. Brown KA, et al. Hum Mol Genet. 1996 Jan;5(1):169-73. doi: 10.1093/hmg/5.1.169. Hum Mol Genet. 1996. PMID: 8789457

3

Human sequences homologous to the gene for the cochlear protein Ocp-II do not map to currently known non-syndromic hearing loss loci.

Brown KA, Leek JP, Lench NJ, Moynihan LM, Markham AF, Mueller RF. Brown KA, et al. Ann Hum Genet. 1996 Sep;60(5):385-9. doi: 10.1111/j.1469-1809.1996.tb00436.x. Ann Hum Genet. 1996. PMID: 8912791

4

A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.

Campbell DA, McHale DP, Brown KA, Moynihan LM, Houseman M, Karbani G, Parry G, Janjua AH, Newton V, al-Gazali L, Markham AF, Lench NJ, Mueller RF. Campbell DA, et al. Among authors: brown ka. J Med Genet. 1997 Dec;34(12):1015-7. doi: 10.1136/jmg.34.12.1015. J Med Genet. 1997. PMID: 9429146 Free PMC article.

5

Comparative genetic mapping for the identification of novel diagnostic and therapeutic targets.

Coletta PL, Lench NJ, Brown KA, Markham AF. Coletta PL, et al. Among authors: brown ka. Curr Opin Biotechnol. 1994 Dec;5(6):643-7. doi: 10.1016/0958-1669(94)90088-4. Curr Opin Biotechnol. 1994. PMID: 7765747 Review.

6

Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type I.

Evans KL, Fantes J, Simpson C, Arveiler B, Muir W, Fletcher J, van Heyningen V, Steel KP, Brown KA, Brown SD, et al. Evans KL, et al. Among authors: brown ka, brown sd. Hum Mol Genet. 1993 Feb;2(2):115-8. doi: 10.1093/hmg/2.2.115. Hum Mol Genet. 1993. PMID: 8499899

7

A type VII myosin encoded by the mouse deafness gene shaker-1.

Gibson F, Walsh J, Mburu P, Varela A, Brown KA, Antonio M, Beisel KW, Steel KP, Brown SD. Gibson F, et al. Among authors: brown ka, brown sd. Nature. 1995 Mar 2;374(6517):62-4. doi: 10.1038/374062a0. Nature. 1995. PMID: 7870172

8

Reverse genetic approaches to cloning deafness genes.

Brown SD, Brown KA, Sutcliffe MJ, Cavanna JS, Greenfield AJ, Steel KP. Brown SD, et al. Among authors: brown ka. Ann N Y Acad Sci. 1991;630:93-9. doi: 10.1111/j.1749-6632.1991.tb19578.x. Ann N Y Acad Sci. 1991. PMID: 1952627 No abstract available.

9

Sequencing of the olfactory marker protein gene in normal and shaker-1 mutant mice.

Brown KA, Sutcliffe MJ, Steel KP, Brown SD. Brown KA, et al. Among authors: brown sd. Mamm Genome. 1994 Jan;5(1):11-4. doi: 10.1007/BF00360561. Mamm Genome. 1994. PMID: 8111122

10

Mouse chromosome 7.

Rinchik EM, Magnuson T, Holdener-Kenny B, Kelsey G, Bianchi A, Conti CJ, Chartier F, Brown KA, Brown SD, Peters J. Rinchik EM, et al. Among authors: brown ka, brown sd. Mamm Genome. 1992;3 Spec No:S104-20. doi: 10.1007/BF00648425. Mamm Genome. 1992. PMID: 1498426 Review. No abstract available.

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