Ngā hua rapu - Albertson, D.

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

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

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

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