Resultats de la cerca - Albertson, D.

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

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

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

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Analysis of a T-cell tumor-specific breakpoint cluster at human chromosome 14q32. per 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. per 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 per 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. per 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. per 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 per 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 per 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 per 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 per 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 per 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 per 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 per 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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