Mueller RF - Search Results

1

Attitudes of deaf adults toward genetic testing for hereditary deafness.

Middleton A, Hewison J, Mueller RF. Middleton A, et al. Among authors: mueller rf. Am J Hum Genet. 1998 Oct;63(4):1175-80. doi: 10.1086/302060. Am J Hum Genet. 1998. PMID: 9758618 Free PMC article.

2

A pilot study of attitudes of deaf and hearing parents towards issues surrounding genetic testing for deafness.

Middleton A, Hewison J, Mueller RF. Middleton A, et al. Among authors: mueller rf. Am J Hum Genet. 1997 Oct;61(4):A190. Am J Hum Genet. 1997. PMID: 11644964 No abstract available.

3

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: mueller rf. Hum Mol Genet. 1997 Nov;6(12):2173-7. doi: 10.1093/hmg/6.12.2173. Hum Mol Genet. 1997. PMID: 9336442

4

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

5

Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing.

Hutchin T, Coy NN, Conlon H, Telford E, Bromelow K, Blaydon D, Taylor G, Coghill E, Brown S, Trembath R, Liu XZ, Bitner-Glindzicz M, Mueller R. Hutchin T, et al. Clin Genet. 2005 Dec;68(6):506-12. doi: 10.1111/j.1399-0004.2005.00539.x. Clin Genet. 2005. PMID: 16283880

6

Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafness.

Moynihan LM, Bundey SE, Heath D, Jones EL, McHale DP, Mueller RF, Markham AF, Lench NJ. Moynihan LM, et al. Among authors: mueller rf. Am J Hum Genet. 1998 May;62(5):1123-8. doi: 10.1086/301824. Am J Hum Genet. 1998. PMID: 9545394 Free PMC article.

7

Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter.

Jackson AP, McHale DP, Campbell DA, Jafri H, Rashid Y, Mannan J, Karbani G, Corry P, Levene MI, Mueller RF, Markham AF, Lench NJ, Woods CG. Jackson AP, et al. Among authors: mueller rf. Am J Hum Genet. 1998 Aug;63(2):541-6. doi: 10.1086/301966. Am J Hum Genet. 1998. PMID: 9683597 Free PMC article.

8

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. Among authors: mueller rf. Hum Mol Genet. 1996 Jan;5(1):169-73. doi: 10.1093/hmg/5.1.169. Hum Mol Genet. 1996. PMID: 8789457

9

A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34.

Moynihan L, Jackson AP, Roberts E, Karbani G, Lewis I, Corry P, Turner G, Mueller RF, Lench NJ, Woods CG. Moynihan L, et al. Among authors: mueller rf. Am J Hum Genet. 2000 Feb;66(2):724-7. doi: 10.1086/302777. Am J Hum Genet. 2000. PMID: 10677332 Free PMC article.

10

Identification of microcephalin, a protein implicated in determining the size of the human brain.

Jackson AP, Eastwood H, Bell SM, Adu J, Toomes C, Carr IM, Roberts E, Hampshire DJ, Crow YJ, Mighell AJ, Karbani G, Jafri H, Rashid Y, Mueller RF, Markham AF, Woods CG. Jackson AP, et al. Among authors: mueller rf. Am J Hum Genet. 2002 Jul;71(1):136-42. doi: 10.1086/341283. Epub 2002 Jun 3. Am J Hum Genet. 2002. PMID: 12046007 Free PMC article.

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