Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ottenheim, C. P. E."'
Autor:
Lakeman, P., van Koningsbruggen, S., Redeker, E. J. W., Ottenheim, C. P. E., Mathijssen, I. B., Cornel, M. C., Mannens, M. M. A. M., Meijers-Heijboer, E. J., Henneman, L.
Publikováno v:
Lakeman, P, van Koningsbruggen, S, Redeker, E J W, Ottenheim, C P E, Mathijssen, I B, Cornel, M C, Mannens, M M A M, Meijers-Heijboer, E J & Henneman, L 2018, ' Evaluation of an expanded carrier screening offer in a non commercial setting ', European Journal of Human Genetics, vol. 26, pp. 82-83 .
European Journal of Human Genetics, 26, 82-83. Nature Publishing Group
European Journal of Human Genetics, 26, 82-83. Nature Publishing Group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5140b6936c4ce0fe0716b249fcc087f8
https://research.vumc.nl/en/publications/d7fe362b-7558-488e-a9c9-bcb58ad0e444
https://research.vumc.nl/en/publications/d7fe362b-7558-488e-a9c9-bcb58ad0e444
Autor:
Brinkmann, J. F. F., Ottenheim, C. P. E., Zegers, R. H. C., de Jong, P. T. V. M., Bergen, A. A. B.
Publikováno v:
Human genetics, 118(6). Springer Verlag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::619598ab788e0ada78d35f808950a12a
https://pure.amc.nl/en/publications/gene-symbol-cyp1b1-disease-glaucoma-primary-congenital-accession-hd0513(41980cbc-e7af-41fd-bb46-c04f0f4b6ef5).html
https://pure.amc.nl/en/publications/gene-symbol-cyp1b1-disease-glaucoma-primary-congenital-accession-hd0513(41980cbc-e7af-41fd-bb46-c04f0f4b6ef5).html
Autor:
Piersma, A. H., Ploemacher, R. E., Brockbank, K. G. M., Nikkels, P. G. J., Ottenheim, C. P. E.
Publikováno v:
Cell Proliferation; Nov1985, Vol. 18 Issue 6, p589-595, 7p
Autor:
Brinkmann, J. F. F., Ottenheim, C. P. E., Jong, L. A. M. S., Zegers, R. H. C., Marc de Smet, Jong, P. T. V. M., Bergen, A. A. B.
Publikováno v:
Scopus-Elsevier
Molecular Vision, 11(68), 582-586. Molecular Vision
Molecular Vision, 11(68), 582-586. Molecular Vision
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c9d6b34aa5bcc5f2b04dc936bb39c4b5
http://www.scopus.com/inward/record.url?eid=2-s2.0-26244431539&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-26244431539&partnerID=MN8TOARS
Autor:
Brinkmann JF; Department of Clinical and Molecular Ophthalmogenetics, Division of Development, Aging and Genetic Diseases of the Eye, The Netherlands Ophthalmic Research Institute, KNAW, Meibergdreef 47, 1105 Amsterdam, The Netherlands. J.Brinkmann@ioi.knaw.nl, Ottenheim CP, Zegers RH, de Jong PT, Bergen AA
Publikováno v:
Human genetics [Hum Genet] 2006 Feb; Vol. 118 (6), pp. 775.