Search Results - "Gschwend, Michele"

Genomewide Scan of Multiple Sclerosis in Finnish Multiplex Families by Kuokkanen, Satu, Gschwend, Michele, Rioux, John D., Daly, Mark J., Terwilliger, Joseph D., Tienari, Pentti J., Wikström, Juhani, Palo, Jorma, Stein, Lincoln D., Hudson, Thomas J., Lander, Eric S., Peltonen, Leena

“…Multiple sclerosis (MS) is a neurological, demyelinating disorder with a putative autoimmune etiology. It is thought to be a multifactorial disease with a…”
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Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect by STINE, O. C, XU, J, VISHIO, E, RISKIN, K, FEILOTTER, H, CHEN, E, SHEN, S, FOLSTEIN, S, MEYERS, D. A, BOTSTEIN, D, MARR, T. G, DEPAULO, J. R, KOSKELA, R, MCMAHON, F. J, GSCHWEND, M, FRIDDLE, C, CLARK, C. D, MCINNIS, M. G, SIMPSON, S. G, BRESCHEL, T. S

“…A susceptibility gene on chromosome 18 and a parent-of-origin effect have been suggested for bipolar affective disorder (BPAD). We have studied 28 nuclear…”
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A locus for Fanconi anemia on 16q determined by homozygosity mapping by GSCHWEND, M, LEVRAN, O, AUERBACH, A. D, BOTSTEIN, D, KRUGLYAK, L, RANADE, K, VERLANDER, P. C, SHEN, S, FAURE, S, WEISSENBACH, J, ALTAY, C, LANDER, E. S

“…We report the results of a genomewide scan using homozygosity mapping to identify genes causing Fanconi anemia, a genetically heterogeneous recessive disorder…”
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The application of homozygosity mapping and simultaneous search to Fanconi anemia by Gschwend, Michele Anne

“…The rapid development of high-resolution genetic maps composed of highly polymorphic markers has led to the genetic mapping of many disease genes. However,…”
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PCR methods of genotyping by Hudson, T J, Clark, C D, Gschwend, M, Justice-Higgins, E

“…Two protocols discuss labeling PCR products with radioactive labels. The PCR products are then analyzed on a denaturing polyacrylamide gel and visualized by…”
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