Zobrazeno 1 - 10
of 248
pro vyhledávání: '"Myers, R H."'
Autor:
Myers, R. H.
Publikováno v:
Philosophy and Phenomenological Research, 1999 Jun 01. 59(2), 281-307.
Externí odkaz:
https://www.jstor.org/stable/2653673
Autor:
Myers, R. H.
Publikováno v:
Ethics, 1994 Oct 01. 105(1), 128-152.
Externí odkaz:
https://www.jstor.org/stable/2382171
Publikováno v:
Biometrika, 1975 Apr 01. 62(1), 71-78.
Externí odkaz:
https://www.jstor.org/stable/2334488
Autor:
Myers, R. H.
Publikováno v:
Technometrics, 1964 Nov 01. 6(4), 343-356.
Externí odkaz:
https://www.jstor.org/stable/1266089
Autor:
Wilk, J. B.1 jwilk@bu.edu, Myers, R. H.1, Pankow, J. S.2, Hunt, S. C.3, Leppert, M. F.3, Freedman, B. I.4, Province, M. A.5, Ellison, R. C.1
Publikováno v:
Annals of Human Genetics. Sep2006, Vol. 70 Issue 5, p566-573. 8p. 4 Charts.
Publikováno v:
Scopus-Elsevier
Left ventricular hypertrophy is associated with an increased risk for cardiovascular disease. The known determinants of left ventricular hypertrophy only partially explain its variability. The purpose of this study was to estimate heritability of lef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e890bed40c80edff396c73b3121af58e
http://hdl.handle.net/11588/645955
http://hdl.handle.net/11588/645955
Autor:
Djoussé, L., Knowlton, B., Hayden, M., Almqvist, E. W., Brinkman, R., Ross, C., Margolis, R., Rosenblatt, A., Durr, A., Dode, C., Morrison, P. J., Andrea Novelletto, Frontali, M., Trent, R. J. A., Mccusker, E., Gómez-Tortosa, E., Mayo, D., Jones, R., Zanko, A., Nance, M., Abramson, R., Suchowersky, O., Paulsen, J., Harrison, M., Yang, Q., Cupples, L. A., Gusella, J. F., Macdonald, M. E., Myers, R. H.
Publikováno v:
Scopus-Elsevier
Huntington disease (HD) is a neurodegenerative disorder caused by the abnormal expansion of CAG repeats in the HD gene on chromosome 4p16.3. Past studies have shown that the size of expanded CAG repeat is inversely associated with age at onset (AO) o
Publikováno v:
Scopus-Elsevier
We evaluated the hypothesis that Huntington disease (HD) is influenced by the normal HD allele by comparing transmission patterns of genetically linked markers at the D4S10 locus in the normal parent against age at onset in the affected offspring. An
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::02c1a3125e6ed255ba33fb08f120cf49
https://europepmc.org/articles/PMC1682222/
https://europepmc.org/articles/PMC1682222/
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
St George Hyslop, P. H., Haines, J. L., Farrer, L. A., Polinsky, R., Van Broeckhoven, C., Goate, A., Crapper McLachlan, D. R., Orr, H., Bruni, A. C., Sorbi††, S., Rainero, I., Foncin, J. F., Pollen, D., Cantu, J. M., Tupler, Rossella, Voskresenskaya, N., Mayeux, R., Growdon, J., Fried, V. A., Myers, R. H., Nee, L., Backhovens, H., Martin, J. J., Rossor, M., Owen, M. J., Mullan, M., Percy, M. E., Karlinsky, H., Rich, S., Heston, L., Montesi, M., Mortilla, M., Nacmias, N., Gusella, J. F., Hardy, J. A.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3674::ce9acc105a7d39c7975829e583cc1808
https://hdl.handle.net/11380/459472
https://hdl.handle.net/11380/459472