Guidelines for investigating causality of sequence variants in human disease von MacArthur, D. G., Manolio, T. A., Dimmock, D. P., Rehm, H. L., Shendure, J., Abecasis, G. R., Adams, D. R., Altman, R. B., Antonarakis, S. E., Ashley, E. A., Barrett, J. C., Biesecker, L. G., Conrad, D. F., Cooper, G. M., Cox, N. J., Daly, M. J., Gerstein, M. B., Goldstein, D. B., Hirschhorn, J. N., Leal, S. M., Pennacchio, L. A., Stamatoyannopoulos, J. A., Sunyaev, S. R., Valle, D., Voight, B. F., Winckler, W., Gunter, C.

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Haplotype analysis of the apolipoprotein gene cluster on humanchromosome 11 von Olivier, M., Wang, X., Cole, R., Gau, B., Kim, J., Rubin, E.M., Pennacchio, L.A.

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Genetics of epilepsy von Pennacchio, L.A.

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Genetics of epilepsy : Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1) von Pennacchio, L.A.

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W06-O-002 Apolipoprotein AV accelerates plasma hydrolysis of triglyceride-rich lipoproteins by interaction with proteoglycan bound lipoprotein lipase von Merkel, M., Loeffler, B., Kluger, M., Fabig, N., Aydin, B., Geppert, G., Pennacchio, L.A., Laatsch, A., Heeren, J.

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Apolipoprotein AIV gene variant S347 is associated with increased risk of coronary heart disease and lower plasma apolipoprotein AIV levels von Wong, W.-M.R, Hawe, E, Li, L.K, Miller, G.J, Nicaud, V, Pennacchio, L.A, Humphries, S.E, Talmud, P.J

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