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Mapping 250K/500K SNP assay

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chapter 1 | Overview 11<br />

23. Schaid, D.J., Guenther, J.C., Christensen, G.B., Hebbring, S.,<br />

Rosenow, C., Hilker, C.A., McDonnell, S.K., Cunningham, J.M.,<br />

Slager, S.L., Blute, M.L., Thibodeau, S.N. Comparison of<br />

microsatellites versus single-nucleotide polymorphisms in a<br />

genome linkage screen for prostate cancer-susceptibility Loci. Am<br />

J Hum Genet 75:948-65 (2004).<br />

24. Sellick, G.S., Garrett, C., Houlston, R.S. A novel gene for neonatal<br />

diabetes maps to chromosome 10p12.1-p13. Diabetes 52:2636-8<br />

(2003).<br />

25. Middleton, F.A., Pato, M.T., Gentile, K.L., Morley, C.P., Zhao,<br />

X., Eisener, A.F., Brown, A., Petryshen, T.L., Kirby, A.N.,<br />

Medeiros, H., Carvalho, C., Macedo, A., Dourado, A., Coelho, I.,<br />

Valente, J., Soares, M.J., Ferreira, C.P., Lei, M., Azevedo, M.H.,<br />

Kennedy, J.L., Daly, M.J., Sklar, P., Pato, C.N. Genomewide<br />

linkage analysis of bipolar disorder by use of a high-density singlenucleotide-polymorphism<br />

(<strong>SNP</strong>) genotyping <strong>assay</strong>: a comparison<br />

with microsatellite marker <strong>assay</strong>s and finding of significant<br />

linkage to chromosome 6q22. Am J Hum Genet 74:886-97 (2004).<br />

26. Shrimpton, A.E., Levinsohn, E.M., Yozawitz, J.M., Packard, D.S.,<br />

Jr., Cady, R.B., Middleton, F.A., Persico, A.M., Hootnick, D.R. A<br />

HOX gene mutation in a family with isolated congenital vertical<br />

talus and Charcot-Marie-Tooth disease. Am J Hum Genet 75:92-6<br />

(2004).<br />

27. Puffenberger, E.G., Hu-Lince, D., Parod, J.M., Craig, D.W., Dobrin,<br />

S.E., Conway, A.R., Donarum, E.A., Strauss, K.A., Dunckley, T.,<br />

Cardenas, J.F., Melmed, K.R., Wright, C.A., Liang, W., Stafford, P.,<br />

Flynn, C.R., Morton, D.H., Stephan, D.A. <strong>Mapping</strong> of sudden infant<br />

death with dysgenesis of the testes syndrome (SIDDT) by a <strong>SNP</strong><br />

genome scan and identification of TSPYL loss of function. Proc Natl<br />

Acad Sci USA 101:11689-94 (2004).<br />

28. Kaindl, A.M., Ruschendorf, F., Krause, S., Goebel, H.H., Koehler,<br />

K., Becker, C., Pongratz, D., Muller-Hocker, J., Nurnberg, P.,<br />

Stoltenburg-Didinger, G., Lochmuller, H., Huebner, A. Missense<br />

mutations of ACTA1 cause dominant congenital myopathy with<br />

cores. J Med Genet 41:842-8 (2004).

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