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CDKN2A common variants and their association with melanoma risk: A population-based study
- Debniak, T., Scott, Rodney J., Huzarski, T., Byrski, T., Rozmiarek, A., Debniak, B., Zaluga, E., Maleszka, R., Kladny, J., Gorski, B., Cybulski, C., Gronwald, J., Kurzawski, G., Lubinski, J.
Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations
- So, J., Suckow, V., Kijas, Z., Kalscheuer, V., Moser, B., Winter, J., Baars, M., Firth, H., Lunt, P., Hamel, B., Meinecke, P., Moraine, C., Odent, S., Schinzel, A., van der Smagt, J. J., Devriendt, K., Albrecht, B., Gillessen-Kaesbach, G., van der Burgt, I., Petrij, F., Faivre, L., McGaughran, J., McKenzie, Fiona, Opitz, J. M., Cox, T., Schweiger, S.
SIAH1 targets the alternative splicing factor T-STAR for degradation by the proteasome
- Venables, Julian P., Dalgliesh, Caroline, Paronetto, Maria Paolo, Skitt, Lindi, Thornton, Jared K., Saunders, Philippa T., Sette, Claudio, Jones, Keith T., Elliott, David J.
Investigation of Nicotiana tabacum (plus) N suaveolens cybrids with carpelloid stamens
- Fitter, John T., Thomas, Mark R., Niu, Chen, Rose, Ray J.
Hereditary haemochromatosis: to screen or not to screen? (editorial)
- Olynyk, J. K., Trinder, D., Milward, Adrienne Elizabeth
A method for meta-analysis of molecular association studies
- Thakkinstian, A., McElduff, P., D'Este, Catherine Anne, Duffy, D., Attia, John Richard
- Avery-Kiejda, Kelly A., Zhang, Xu Dong, Adams, Luke J., Scott, Rodney J., Vojtesek, Borivoj, Lane, David P., Hersey, Peter
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