Molecular markers near two mouse Chromosome 13 genes, muted and pearl, which cause platelet storage pool deficiency (SPD)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00350888.pdf
Reference36 articles.
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3. Bennett, J.S., Kolodziej, M.A. (1992). Disorders of platelet function. Disease-a-Month 38, 580?631.
4. Dietrich, W.F., Miller, J.C., Steen, R.G., Merchant, M., Damron, D., Nahf, R., Joyce, D.C., Dredge, R.D., Marquis, A., Stein, L.D., Goodman, N., Page, D.C., Lander, E.S. (1994). A genetic map of the mouse with 3012 simple sequence length polymorphisms. Nature Genet. 7, 220?245. Supplemented by additional markers in: Whitehead Institute/MIT Center for Genome Research, Genetic Map of the Mouse, Database Release 6, 1994.
5. Douville, P., Seldin, M.F., Carbonetto, S. (1992). Genetic mapping of the integrin a1 gene (Vla1) to mouse chromosome 13. Genomics 14, 503?505.
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2. Abnormal Expression and Subcellular Distribution of Subunit Proteins of the AP-3 Adaptor Complex Lead to Platelet Storage Pool Deficiency in the Pearl Mouse;Blood;1999-07-01
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