Houseman MJ - Search Results

1

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene.

Denoyelle F, Weil D, Maw MA, Wilcox SA, Lench NJ, Allen-Powell DR, Osborn AH, Dahl HH, Middleton A, Houseman MJ, Dodé C, Marlin S, Boulila-ElGaïed A, Grati M, Ayadi H, BenArab S, Bitoun P, Lina-Granade G, Godet J, Mustapha M, Loiselet J, El-Zir E, Aubois A, Joannard A, Levilliers J, Garabédian EN, Mueller RF, Gardner RJ, Petit C, et al. Denoyelle F, et al. Among authors: houseman mj. Hum Mol Genet. 1997 Nov;6(12):2173-7. doi: 10.1093/hmg/6.12.2173. Hum Mol Genet. 1997. PMID: 9336442

2

DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qter.

Moynihan L, Houseman M, Newton V, Mueller R, Lench N. Moynihan L, et al. Eur J Hum Genet. 1999 Feb-Mar;7(2):243-6. doi: 10.1038/sj.ejhg.5200269. Eur J Hum Genet. 1999. PMID: 10196710

3

Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss.

Houseman MJ, Ellis LA, Pagnamenta A, Di WL, Rickard S, Osborn AH, Dahl HH, Taylor GR, Bitner-Glindzicz M, Reardon W, Mueller RF, Kelsell DP. Houseman MJ, et al. J Med Genet. 2001 Jan;38(1):20-5. doi: 10.1136/jmg.38.1.20. J Med Genet. 2001. PMID: 11134236 Free PMC article.

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. 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

Connexin-26 mutations in sporadic non-syndromal sensorineural deafness.

Lench N, Houseman M, Newton V, Van Camp G, Mueller R. Lench N, et al. Lancet. 1998 Feb 7;351(9100):415. doi: 10.1016/s0140-6736(98)24006-2. Lancet. 1998. PMID: 9482297 No abstract available.

6

A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31.

Pulleyn LJ, Jackson AP, Roberts E, Carridice A, Muxworthy C, Houseman M, Al-Gazali LI, Lench NJ, Markham AF, Mueller RF. Pulleyn LJ, et al. Eur J Hum Genet. 2000 Dec;8(12):991-3. doi: 10.1038/sj.ejhg.5200567. Eur J Hum Genet. 2000. PMID: 11175289

7

Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations--molecular and audiological findings.

Mueller RF, Nehammer A, Middleton A, Houseman M, Taylor GR, Bitner-Glindzciz M, Van Camp G, Parker M, Young ID, Davis A, Newton VE, Lench NJ. Mueller RF, et al. Int J Pediatr Otorhinolaryngol. 1999 Oct 15;50(1):3-13. doi: 10.1016/s0165-5876(99)00242-6. Int J Pediatr Otorhinolaryngol. 1999. PMID: 10596881

8

A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.

Van Laer L, Coucke P, Mueller RF, Caethoven G, Flothmann K, Prasad SD, Chamberlin GP, Houseman M, Taylor GR, Van de Heyning CM, Fransen E, Rowland J, Cucci RA, Smith RJ, Van Camp G. Van Laer L, et al. J Med Genet. 2001 Aug;38(8):515-8. doi: 10.1136/jmg.38.8.515. J Med Genet. 2001. PMID: 11483639 Free PMC article.

9

A novel mutation in a family with non-syndromic sensorineural hearing loss that disrupts the newly characterised OTOF long isoforms.

Houseman MJ, Jackson AP, Al-Gazali LI, Badin RA, Roberts E, Mueller RF. Houseman MJ, et al. J Med Genet. 2001 Aug;38(8):E25. doi: 10.1136/jmg.38.8.e25. J Med Genet. 2001. PMID: 11483641 Free PMC article. No abstract available.

10

Connexin mutations in skin disease and hearing loss.

Kelsell DP, Di WL, Houseman MJ. Kelsell DP, et al. Among authors: houseman mj. Am J Hum Genet. 2001 Mar;68(3):559-68. doi: 10.1086/318803. Epub 2001 Jan 25. Am J Hum Genet. 2001. PMID: 11179004 Free PMC article. Review. No abstract available.

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