Your selections:
Planning the Human Variome Project: the Spain report
- Kaput, Jim, Cotton, Richard G. H., Bapat, Bharati, Bernstein, Inge T., Bhak, Jong, Bleoo, Stacey L., Blöcker, Helmut, Brenner, Steven E., Burn, John, Bustamante, Mariona, Calzone, Rita, Scott, Rodney J., Hardman, Lauren, Watson, Michael, Aqeel, Aida I. Al, Al-Aama, Jumana Y., Al-Mulla, Fahd, Alonso, Santos, Aretz, Stefan, Auerbach, Arleen D.
A novel missense LIPA gene mutation, N98S, in a patient with cholesteryl ester storage disease
- Hooper, Amanda J., Tran, Huy A., Formby, Mark R., Burnett, John R.
- Avery-Kiejda, Kelly A., Zhang, Xu Dong, Adams, Luke J., Scott, Rodney J., Vojtesek, Borivoj, Lane, David P., Hersey, Peter
Variable phenotypic expression in HNPCC and the search for modifier genes
- Tzircotis, G., Thorne, R. F., Isacke, C. M.
Hereditary haemochromatosis: to screen or not to screen? (editorial)
- Olynyk, J. K., Trinder, D., Milward, Adrienne Elizabeth
Phenotype-genotype correlations in a series of Wolfram syndrome families
- Smith, Casey J. A., Crock, Patricia A., King, Bruce R., Meldrum, Cliff J., Scott, Rodney J.
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