Arama Sonuçları - Stetten, G

Clonal evolution in human lymphoblast cultures. Yazar: Migeon, B R, Axelman, J, Stetten, G

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Translocation of the nucleolus organizer region to the human X chromosome. Yazar: Stetten, G, Sroka, B, Schmidt, M, Axelman, J, Migeon, B R

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Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia. Yazar: Latt, S A, Stetten, G, Juergens, L A, Buchanan, G R, Gerald, P S

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TRPC1, a human homolog of a Drosophila store-operated channel. Yazar: Wes, P D, Chevesich, J, Jeromin, A, Rosenberg, C, Stetten, G, Montell, C

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Molecular mechanism in the formation of a human ring chromosome 21. Yazar: Wong, C, Kazazian, H H, Stetten, G, Earnshaw, W C, Van Keuren, M L, Antonarakis, S E

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Chromosomal disorders: background and neuroradiology. Yazar: Kumar, A J, Naidich, T P, Stetten, G, Reiss, A L, Wang, H, Thomas, G H, Hurko, O

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Analysis of reciprocal translocations by chromosome painting: applications and limitations of the technique. Yazar: Rosenberg, C, Blakemore, K J, Kearns, W G, Giraldez, R A, Escallon, C S, Pearson, P L, Stetten, G

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Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study Yazar: Graf, M D, Christ, L, Mascarello, J T, Mowrey, P, Pettenati, M, Stetten, G, Storto, P, Surti, U, Van Dyke, D L, Vance, G H, Wolff, D, Schwartz, S

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Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21 Yazar: McGinniss, M. J., Kazazian, H. H., Stetten, G., Petersen, M. B., Boman, H., Engel, E., Greenberg, F., Hertz, J. M., Johnson, A., Laca, Z., Mikkelsen, M., Patil, S. R., Schinzel, A. A., Tranebjaerg, L., Antonarakis, S. E.

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