Torthaí cuardaigh - Albertson, D.
- 1 - 16 toradh as 16 á dtaispeáint
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Mapping muscle protein genes by in situ hybridization using biotin-labeled probes. de réir Albertson, D G
Foilsithe / Cruthaithe 1985Téacs -
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Analysis of a T-cell tumor-specific breakpoint cluster at human chromosome 14q32. de réir Mengle-Gaw, L, Albertson, D G, Sherrington, P D, Rabbitts, T H
Foilsithe / Cruthaithe 1988Téacs -
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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. de réir Albertson, D G, Fishpool, R, Sherrington, P, Nacheva, E, Milstein, C
Foilsithe / Cruthaithe 1988Téacs -
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BAC microarray analysis of 15q11–q13 rearrangements and the impact of segmental duplications de réir Locke, D, Segraves, R, Nicholls, R, Schwartz, S, Pinkel, D, Albertson, D, Eichler, E
Foilsithe / Cruthaithe 2004Téacs -
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RFLP and mapping of human MOX-1 gene on chromosome 3. de réir Douglas, J, Albertson, D G, Barclay, A N, Davis, M, Rabbitts, P H
Foilsithe / Cruthaithe 1988Téacs -
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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. de réir Buluwela, L, Albertson, D G, Sherrington, P, Rabbitts, P H, Spurr, N, Rabbitts, T H
Foilsithe / Cruthaithe 1988Téacs -
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Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1 de réir Slavotinek, A, Lee, S, Davis, R, Shrit, A, Leppig, K, Rhim, J, Jasnosz, K, Albertson, D, Pinkel, D
Foilsithe / Cruthaithe 2005Téacs -
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A large field CCD system for quantitative imaging of microarrays de réir Hamilton, G., Brown, N., Oseroff, V., Huey, B., Segraves, R., Sudar, D., Kumler, J., Albertson, D., Pinkel, D.
Foilsithe / Cruthaithe 2006Téacs -
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The Histopathology of Oral Cancer Pain in a Mouse Model and a Human Cohort de réir Naik, K., Janal, M.N., Chen, J., Bandary, D., Brar, B., Zhang, S., Dolan, J.C., Schmidt, B.L., Albertson, D.G., Bhattacharya, A.
Foilsithe / Cruthaithe 2020Téacs -
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Genome wide array comparative genomic hybridisation analysis of premalignant lesions of the stomach de réir 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
Foilsithe / Cruthaithe 2003Téacs -
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Canine urothelial carcinoma: genomically aberrant and comparatively relevant de réir 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.
Foilsithe / Cruthaithe 2015Téacs -
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Two molecular cytogenetic views of breast cancer de réir 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
Foilsithe / Cruthaithe 2000Téacs -
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Integration of cytogenetic landmarks into the draft sequence of the human genome de réir 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.
Foilsithe / Cruthaithe 2001Téacs