A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity-Reference-Cited by-同舟云学术

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A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity

Published:2005-12-05 Issue:2 Volume:15 Page:251-258
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Lee Hane,Jen Joanna C.,Wang Hui,Chen Zugen,Mamsa Hafsa,Sabatti Chiara,Baloh Robert W.,Nelson Stanley F.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/15/2/251/1620121/ddi441.pdf

Reference46 articles.

1. Kroenke, K. and Price, R.K. (1993) Symptoms in the community. Prevalence, classification, and psychiatric comorbidity. Arch. Intern. Med., 153, 2474–2480.

2. Baloh, R.W. (1998) Vertigo. Lancet, 352, 1841–1846.

3. Oh, A.K., Lee, H., Jen, J.C., Corona, S., Jacobson, K.M. and Baloh, R.W. (2001) Familial benign recurrent vertigo. Am. J. Med. Genet., 100, 287–291.

4. John, S., Shephard, N., Liu, G., Zeggini, E., Cao, M., Chen, W., Vasavda, N., Mills, T., Barton, A., Hinks, A. et al. (2004) Whole-genome scan, in a complex disease, using 11 245 single-nucleotide polymorphisms: comparison with microsatellites. Am. J. Hum. Genet., 75, 54–64.

5. Middleton, F.A., Pato, M.T., Gentile, K.L., Morley, C.P., Zhao, X., Eisener, A.F., Brown, A., Petryshen, T.L., Kirby, A.N., Medeiros, H. et al. (2004) Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22. Am. J. Hum. Genet., 74, 886–897.

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