Hakutulokset - Albertson, D.

Mapping Chromosome Rearrangement Breakpoints to the Physical Map of Caenorhabditis Elegans by Fluorescent in Situ Hybridization Tekijä Albertson, D. G.

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Mapping muscle protein genes by in situ hybridization using biotin-labeled probes. Tekijä Albertson, D G

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Localization of the ribosomal genes in Caenorhabditis elegans chromosomes by in situ hybridization using biotin-labeled probes. Tekijä Albertson, D G

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Isolation of Dominant Xo-Feminizing Mutations in Caenorhabditis Elegans: New Regulatory Tra Alleles and an X Chromosome Duplication with Implications for Primary Sex Determination Tekijä Hodgkin, J., Albertson, D. G.

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Analysis of a T-cell tumor-specific breakpoint cluster at human chromosome 14q32. Tekijä Mengle-Gaw, L, Albertson, D G, Sherrington, P D, Rabbitts, T H

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Sensitive and high resolution in situ hybridization to human chromosomes using biotin labelled probes: assignment of the human thymocyte CD1 antigen genes to chromosome 1. Tekijä Albertson, D G, Fishpool, R, Sherrington, P, Nacheva, E, Milstein, C

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BAC microarray analysis of 15q11–q13 rearrangements and the impact of segmental duplications Tekijä Locke, D, Segraves, R, Nicholls, R, Schwartz, S, Pinkel, D, Albertson, D, Eichler, E

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RFLP and mapping of human MOX-1 gene on chromosome 3. Tekijä Douglas, J, Albertson, D G, Barclay, A N, Davis, M, Rabbitts, P H

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The use of chromosomal translocations to study human immunoglobulin gene organization: mapping DH segments within 35 kb of the C mu gene and identification of a new DH locus. Tekijä Buluwela, L, Albertson, D G, Sherrington, P, Rabbitts, P H, Spurr, N, Rabbitts, T H

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Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1 Tekijä Slavotinek, A, Lee, S, Davis, R, Shrit, A, Leppig, K, Rhim, J, Jasnosz, K, Albertson, D, Pinkel, D

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A large field CCD system for quantitative imaging of microarrays Tekijä Hamilton, G., Brown, N., Oseroff, V., Huey, B., Segraves, R., Sudar, D., Kumler, J., Albertson, D., Pinkel, D.

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The Histopathology of Oral Cancer Pain in a Mouse Model and a Human Cohort Tekijä Naik, K., Janal, M.N., Chen, J., Bandary, D., Brar, B., Zhang, S., Dolan, J.C., Schmidt, B.L., Albertson, D.G., Bhattacharya, A.

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Genome wide array comparative genomic hybridisation analysis of premalignant lesions of the stomach Tekijä Weiss, M M, Kuipers, E J, Postma, C, Snijders, A M, Stolte, M, Vieth, M, Pinkel, D, Meuwissen, S G M, Albertson, D, Meijer, G A

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Canine urothelial carcinoma: genomically aberrant and comparatively relevant Tekijä Shapiro, S. G., Raghunath, S., Williams, C., Motsinger-Reif, A. A., Cullen, J. M., Liu, T., Albertson, D., Ruvolo, M., Lucas, A. Bergstrom, Jin, J., Knapp, D. W., Schiffman, J. D., Breen, M.

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Two molecular cytogenetic views of breast cancer Tekijä Gray, J, Chin, K, Collins, C, Yaswin, P, Nonet, G, Kowbel, D, Kuo, W-L, Garcia, E, Ortiz de Solorzano, C, Knowles, D, Lockett, S, Bissell, M, Weaver, V, Pinkel, D, Albertson, D, Børresen-Dale, A-L, Waldnian, F

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Integration of cytogenetic landmarks into the draft sequence of the human genome Tekijä BAC Resource Consortium, The, Cheung, V. G., Nowak, N., Jang, W., Kirsch, I. R., Zhao, S., Chen, X.-N., Furey, T. S., Kim, U.-J., Kuo, W.-L., Olivier, M., Conroy, J., Kasprzyk, A., Massa, H., Yonescu, R., Sait, S., Thoreen, C., Snijders, A., Lemyre, E., Bailey, J. A., Bruzel, A., Burrill, W. D., Clegg, S. M., Collins, S., Dhami, P., Friedman, C., Han, C. S., Herrick, S., Lee, J., Ligon, A. H., Lowry, S., Morley, M., Narasimhan, S., Osoegawa, K., Peng, Z., Plajzer-Frick, I., Quade, B. J., Scott, D., Sirotkin, K., Thorpe, A. A., Gray, J. W., Hudson, J., Pinkel, D., Ried, T., Rowen, L., Shen-Ong, G. L., Strausberg, R. L., Birney, E., Callen, D. F., Cheng, J.-F., Cox, D. R., Doggett, N. A., Carter, N. P., Eichler, E. E., Haussler, D., Korenberg, J. R., Morton, C. C., Albertson, D., Schuler, G., de Jong, P. J., Trask, B. J.

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