Newton V - Search Results

1

Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB.

Lévy G, Levi-Acobas F, Blanchard S, Gerber S, Larget-Piet D, Chenal V, Liu XZ, Newton V, Steel KP, Brown SD, Munnich A, Kaplan J, Petit C, Weil D. Lévy G, et al. Among authors: newton v. Hum Mol Genet. 1997 Jan;6(1):111-6. doi: 10.1093/hmg/6.1.111. Hum Mol Genet. 1997. PMID: 9002678

2

Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.

Liu XZ, Hope C, Walsh J, Newton V, Ke XM, Liang CY, Xu LR, Zhou JM, Trump D, Steel KP, Bundey S, Brown SD. Liu XZ, et al. Among authors: newton v. Am J Hum Genet. 1998 Sep;63(3):909-12. doi: 10.1086/302026. Am J Hum Genet. 1998. PMID: 9718356 Free PMC article. No abstract available.

3

Identification of a new mutation of the myosin VII head region in Usher syndrome type 1.

Liu XZ, Newton VE, Steel KP, Brown SD. Liu XZ, et al. Among authors: newton ve. Hum Mutat. 1997;10(2):168-70. doi: 10.1002/(SICI)1098-1004(1997)10:2<168::AID-HUMU10>3.0.CO;2-Y. Hum Mutat. 1997. PMID: 9259201 No abstract available.

4

Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.

Ouyang XM, Yan D, Du LL, Hejtmancik JF, Jacobson SG, Nance WE, Li AR, Angeli S, Kaiser M, Newton V, Brown SD, Balkany T, Liu XZ. Ouyang XM, et al. Among authors: newton v. Hum Genet. 2005 Mar;116(4):292-9. doi: 10.1007/s00439-004-1227-2. Epub 2005 Jan 20. Hum Genet. 2005. PMID: 15660226

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

Distortion product emissions in normal-hearing and low-frequency hearing loss carriers of genes for Waardenburg's syndrome.

Liu XZ, Newton VE. Liu XZ, et al. Among authors: newton ve. Ann Otol Rhinol Laryngol. 1997 Mar;106(3):220-5. doi: 10.1177/000348949710600307. Ann Otol Rhinol Laryngol. 1997. PMID: 9078934

7

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

8

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

9

The mutational spectrum in Waardenburg syndrome.

Tassabehji M, Newton VE, Liu XZ, Brady A, Donnai D, Krajewska-Walasek M, Murday V, Norman A, Obersztyn E, Reardon W, et al. Tassabehji M, et al. Among authors: newton ve. Hum Mol Genet. 1995 Nov;4(11):2131-7. doi: 10.1093/hmg/4.11.2131. Hum Mol Genet. 1995. PMID: 8589691

10

USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian allele.

Ouyang XM, Hejtmancik JF, Jacobson SG, Xia XJ, Li A, Du LL, Newton V, Kaiser M, Balkany T, Nance WE, Liu XZ. Ouyang XM, et al. Among authors: newton v. Clin Genet. 2003 Feb;63(2):150-3. doi: 10.1046/j.0009-9163.2002.00004.x. Clin Genet. 2003. PMID: 12630964

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