Isolation, Characterization, and Precise Physical Localization of Human CDX1, a caudal-Type Homeobox Gene von Bonner, Cynthia A., Loftus, Stacie K., Wasmuth, John J.

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Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes von Zhang, T.W., Choi, J., Kovacs, M.A., Shi, J.X., Xu, M., Goldstein, A.M., Trower, A.J., Bishop, D.T., Iles, M.M., Duffy, D.L., MacGregor, S., Amundadottir, L.T., Law, M.H., Loftus, S.K., Pavan, W.J., Brown, K.M.

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Cloning of the human heparan sulfate- N-deacetylase/ N-sulfotransferase gene from the treacher Collins syndrome candidate region at 5q32–q33.1 von Dixon, Jill, Loftus, Stacie K., Gladwin, Amanda J., Scambler, Peter J., Wasmuth, John J., Dixon, Michael J.

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Genomic Organization of the Human Heparan Sulfate-N-Deacetylase/N-Sulfotransferase Gene: Exclusion from a Causative Role in the Pathogenesis of Treacher Collins Syndrome von Gladwin, Amanda J., Dixon, Jill, Loftus, Stacie K., Wasmuth, John J., Dixon, Michael J.

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A YAC contig encompassing the Treacher Collins syndrome critical region at 5q31. 3-32 von Dixon, J., Gladwin, A.J., Perveen, R., Dixon, M.J., Loftus, S.K., Wasmuth, J.J., Riley, J.H., Anand, R.

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A multi-institutional analysis of intraoperative radiotherapy for early breast cancer: Does age matter? von Abbott, A.M., Valente, S.A., Loftus, L., Tendulkar, R.D., Greif, J.M., Bethke, K.P., Donnelly, E.D., Lottich, C., Ross, D.L., Friedman, N.B., Bedi, C.G., Joh, J.E., Kelemen, P., Hoefer, R.A., Kang, S.K., Ruffer, J., Police, A., Fyles, A., Graves, G.M., Willey, S.C., Tousimis, E.A., Small, W., Lyons, J., Grobmyer, S., Laronga, C.

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