Changes in yearly birth prevalence rates of children with Down syndrome in the period 1986-2007 in the Netherlands

Autor: van de Graaf, G (Gert), Haveman, M, Hochstenbach, R, Engelen, J, Gerssen-Schoorl, K, Poddighe, P, Smeets, D, van Hove, G

Publikováno v: Journal of Intellectual Disability Research, 55, 462-473
Journal of Intellectual Disability Research, 55, 462-473. Wiley-Blackwell
Journal of Intellectual Disability Research, 55(5), 462-473. Wiley
Journal of Intellectual Disability Research, 55, pp. 462-473
Journal of Intellectual Disability Research, 55, 462-473. Wiley-Blackwell Publishing Ltd

Background The Netherlands are lacking reliable national empirical data in relation to the development of birth prevalence of Down syndrome. Our study aims at assessing valid national live birth prevalence rates for the period 1986-2007. Method On th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3699cf5e88f5e2ae20cd6666c9ffcaac
http://hdl.handle.net/2066/95712

Risicofactoren voor structurele chromosoomafwijking bij 2 of meer miskramen als instrument voor selectieve karyotypering

Autor: Franssen, M. T. M., Korevaar, J. C., Leschot, N. J., Bossuyt, P. M. M., Knegt, A. C., Gerssen-Schoorl, K. B. J., Wouters, C. H., Hansson, K. B. M., Hochstenbach, P. F. R., Madan, K., van der Veen, F., Goddijn, M.

Publikováno v: Nederlands tijdschrift voor geneeskunde, 151(15), 863-867. Bohn Stafleu van Loghum

OBJECTIVE: To identify additional risk factors and the corresponding probability of carrying a chromosome abnormality in couples with two or more miscarriages. DESIGN: Nested case-control study. METHOD: In 6 centres for clinical genetics in the Nethe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=narcis______::f4d3394d8e3d0e62e6a234c25a366868
https://pure.amc.nl/en/publications/risicofactoren-voor-structurele-chromosoomafwijking-bij-2-of-meer-miskramen-als-instrument-voor-selectieve-karyotypering(80f3f99d-f4e3-41da-96a8-f95cb9c6ba0c).html

Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience.

Autor: Tuerlings, J H A M, de France, H F, Hamers, A, Hordijk, R, Van Hemel, J O, Hansson, K, Hoovers, J M N, Madan, K, Van Der Blij-Philipsen, M, Gerssen-Schoorl, K B J, Kremer, J A M, Smeets, D F C M

Publikováno v: European Journal of Human Genetics; May98, Vol. 6 Issue 3, p194, 7p

At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocation.

Autor: Smeets, D, van Ravenswaaij, C, de Pater, J, Gerssen-Schoorl, K, Van Hemel, J, Janssen, G, Smits, A

Publikováno v: Journal of Medical Genetics; Jan1997, Vol. 34 Issue 1, p18-23, 6p, 2 Black and White Photographs, 1 Diagram, 1 Chart

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