Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Wapenaar, M. C."'
Autor:
SCHAEFER L, FERRERO G. B, GRILLO A, BASSI M. T, ROTH E. J, WAPENAAR M. C, VAN OMMEN G. J. B, MOHANDAS T. K, ROCCHI M, ZOGHBI H. Y, BALLABIO, ANDREA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::0c9857f952c9f291e6b9ae398d4d7f16
http://hdl.handle.net/11588/130737
http://hdl.handle.net/11588/130737
Akademický článek
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Autor:
Diosdado, B., Wapenaar, M. C., Franke, I., Duran, K. J., Goerres, M. J., Hadithi, M., Crusius, J. B. A., Meijer, J. W. R., Duggan, D. J., Mulder, C. J. J., Holstege, F. C. P., Wijmenga, C.
Publikováno v:
Gut; Jul2004, Vol. 53 Issue 7, p944-951, 7p, 1 Diagram, 4 Charts
Autor:
Laing, N. G., Walker, A. P., Akkari, P. A., Chandler, D. C., Layton, M. G., Mears, M. E., Yamada, T., Bartlett, R. J., Pericak-Vance, M. A., Hung, W.-Y., Wapenaar, M. C., van Ommen, G., Roses, A. D., Kakulas, B. A.
Publikováno v:
Prenatal Diagnosis; Jan1991, Vol. 11 Issue 1, p63-67, 5p
Autor:
Bartlett, R J, Pericak-Vance, M A, Koh, J, Yamaoka, L H, Chen, J C, Hung, W Y, Speer, M C, Wapenaar, M C, Van Ommen, G J, Bakker, E
Publikováno v:
Neurology; Jan1988, Vol. 38 Issue 1, p1-4, 4p
Autor:
Bartlett, R. J., Pericak-Vance, M. A., Koh, J., Yamaoka, L. H., Chen, J. C., Hung, W. -Y., Speer, M. C., Wapenaar, M. C., B. Van Ommen, G. J., Bakker, E., Pearson, P. L., Kandt, R. S., Siddique, T., Gilbert, J. R., Lee, J. E., Sirotkin-Roses, M. J., Roses, A. D.
Publikováno v:
Neurology; Jan1988, Vol. 38 Issue 1, p1-4, 4p
Publikováno v:
Journal of Neurology; December 1989, Vol. 236 Issue: 8 p470-473, 4p
Autor:
Hofker, M. H., Wapenaar, M. C., Goor, Nicole, Bakker, E., van Ommen, G. -J. B., Pearson, P. L.
Publikováno v:
Human Genetics; June 1985, Vol. 70 Issue: 2 p148-156, 9p
Autor:
Wapenaar, M. C., Schiaffino, M. V., Bassi, M. T., Schaefer, L., Chinault, A. C., Zoghbi, H. Y., Andrea BALLABIO
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::daced3c76a3b1e6dd4e0fb514ad776b6
http://www.scopus.com/inward/record.url?eid=2-s2.0-0028240483&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0028240483&partnerID=MN8TOARS
Autor:
Hofker, M. H., Skraastad, M. I., Arthur Bergen, Wapenaar, M. C., Bakker, E., Millington-Ward, A., Ommen, G. J., Pearson, P. L.
Publikováno v:
American journal of human genetics, 39(4), 438-451. Cell Press
Scopus-Elsevier
Scopus-Elsevier
Using a standard technique, 122 single-copy probes were screened for their ability to detect restriction fragment length polymorphisms (RFLPs) in the human genome. The use of a standardized RFLP screening enables the introduction of statistical metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::2feb558d02fbb2123d37080d86a3aeb2
https://pure.amc.nl/en/publications/the-x-chromosome-shows-less-genetic-variation-at-restriction-sites-than-the-autosomes(9d271975-eb07-4ff0-b6ac-9304a687de7f).html
https://pure.amc.nl/en/publications/the-x-chromosome-shows-less-genetic-variation-at-restriction-sites-than-the-autosomes(9d271975-eb07-4ff0-b6ac-9304a687de7f).html