Newton V - Search Results

1

Guidelines and recommendations for testing of Cx26 mutations and interpretation of results.

Mazzoli M, Newton V, Murgia A, Bitner-Glindzicz M, Gasparini P, Read A, Parving A. Mazzoli M, et al. Among authors: newton v. Int J Pediatr Otorhinolaryngol. 2004 Nov;68(11):1397-8. doi: 10.1016/j.ijporl.2004.05.011. Int J Pediatr Otorhinolaryngol. 2004. PMID: 15488970 No abstract available.

2

Hearing loss and pigmentary disturbances in Waardenburg syndrome with reference to WS type II.

Liu X, Newton V, Read A. Liu X, et al. Among authors: newton v. J Laryngol Otol. 1995 Feb;109(2):96-100. doi: 10.1017/s002221510012938x. J Laryngol Otol. 1995. PMID: 7706933

3

Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairment.

Hutchin TP, Thompson KR, Parker M, Newton V, Bitner-Glindzicz M, Mueller RF. Hutchin TP, et al. Among authors: newton v. J Med Genet. 2001 Apr;38(4):229-31. doi: 10.1136/jmg.38.4.229. J Med Genet. 2001. PMID: 11283203 Free PMC article.

4

Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene.

Tassabehji M, Newton VE, Read AP. Tassabehji M, et al. Among authors: newton ve. Nat Genet. 1994 Nov;8(3):251-5. doi: 10.1038/ng1194-251. Nat Genet. 1994. PMID: 7874167

5

Waardenburg syndrome type II: phenotypic findings and diagnostic criteria.

Liu XZ, Newton VE, Read AP. Liu XZ, et al. Among authors: newton ve. Am J Med Genet. 1995 Jan 2;55(1):95-100. doi: 10.1002/ajmg.1320550123. Am J Med Genet. 1995. PMID: 7702105 Review.

6

Waardenburg syndrome.

Read AP, Newton VE. Read AP, et al. Among authors: newton ve. J Med Genet. 1997 Aug;34(8):656-65. doi: 10.1136/jmg.34.8.656. J Med Genet. 1997. PMID: 9279758 Free PMC article. Review.

7

A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1.

Hughes AE, Newton VE, Liu XZ, Read AP. Hughes AE, et al. Among authors: newton ve. Nat Genet. 1994 Aug;7(4):509-12. doi: 10.1038/ng0894-509. Nat Genet. 1994. PMID: 7951321

8

Localization of a gene for Waardenburg syndrome type I.

Read AP, Foy C, Newton V, Harris R. Read AP, et al. Among authors: newton v. Ann N Y Acad Sci. 1991;630:143-51. doi: 10.1111/j.1749-6632.1991.tb19583.x. Ann N Y Acad Sci. 1991. PMID: 1952585 No abstract available.

9

Mapping of DFN2 to Xq22.

Tyson J, Bellman S, Newton V, Simpson P, Malcolm S, Pembrey ME, Bitner-Glindzicz M. Tyson J, et al. Among authors: newton v. Hum Mol Genet. 1996 Dec;5(12):2055-60. doi: 10.1093/hmg/5.12.2055. Hum Mol Genet. 1996. PMID: 8968763

10

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. Among authors: newton ve. 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

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