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  1. 2007

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

    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., 2007, In: Nederlands tijdschrift voor geneeskunde. 151, 15, p. 863-867

    Research output: Contribution to journal › Article › Professional

  3. 2006

  4. Communication with patients during the prenatal testing procedure: an explorative qualitative study

    van Zwieten, M., Willems, D., Knegt, L. & Leschot, N., 2006, In: Patient education and counseling. 63, 1-2, p. 161-168

    Research output: Contribution to journal › Article › Academic › peer-review

  5. 2005

  6. Increased nuchal translucency and split-hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locus

    Bijlsma, E. K., Knegt, A. C., Bilardo, C. M. & Goodman, F. R., 2005, In: Prenatal diagnosis. 25, 1, p. 39-44

    Research output: Contribution to journal › Article › Academic › peer-review

  7. Increased nuchal translucency thickness: a marker for chromosomal and genetic disorders in both offspring and parents

    van Huizen, M. E., Pighetti, M., Bijlsma, E. K., Knegt, A. C. & Bilardo, C. M., 2005, In: Ultrasound in obstetrics & gynecology. 26, 7, p. 793-794

    Research output: Contribution to journal › Comment/Letter to the editor › Academic

  8. Selective chromosome analysis in couples with two or more miscarriages: case-control study

    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, R., Madan, K., van der Veen, F. & Goddijn, M., 2005, In: BMJ (Clinical research ed.). 331, 7509, p. 137-139

    Research output: Contribution to journal › Article › Academic › peer-review

  9. 2004

  10. Reciprocal translocation carriers in recurrent miscarriage parents may yield an unbalanced fetal chromosome pattern (multiple letters) [2]

    Sugiura-Ogasawara, M., Goddijn, M., Joosten, H., Knegt, L., van der Veen, F., Franssen, M., Bonsel, G. & Leschot, N., Sep 2004, In: Human Reproduction. 19, 9, p. 2171-2172 2 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  11. Clinical relevance of diagnosing structural chromosome abnormalities in couples with repeated miscarriage

    Goddijn, M., Joosten, J. H. K., Knegt, A. C., van derVeen, F., Franssen, M. T. M., Bonsel, G. J. & Leschot, N. J., 2004, In: Human reproduction (Oxford, England). 19, 4, p. 1013-1017

    Research output: Contribution to journal › Article › Academic › peer-review

  12. Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two cases

    van Huizen, M. E., Knegt, A. C., Bijlsma, E. K. & Bilardo, C. M., 2004, In: Prenatal diagnosis. 24, 12, p. 1020-1021

    Research output: Contribution to journal › Comment/Letter to the editor › Academic

  13. Invasieve prenatale diagnostiek in Nederland, 1991-2000: aantallen ingrepen, indicaties, en gevonden afwijkingen

    Nagel, H. T. C., Knegt, A. C., Kloosterman, M. D., Wildschut, H. I. J., Leschot, N. J. & Vandenbussche, F. P. H. A., 2004, In: Nederlands tijdschrift voor geneeskunde. 148, 31, p. 1538-1543

    Research output: Contribution to journal › Article › Professional

  14. Reciprocal translocation carriers ascertained for recurrent miscarriage have a possibility to yield an unbalanced fetal chromosome pattern - Reply

    Goddijn, M., Joosten, H., Knegt, L., van der Veen, F., Franssen, M., Bonsel, G. & Leschot, N., 2004, In: Human reproduction (Oxford, England). 19, 9, p. 2172

    Research output: Contribution to journal › Comment/Letter to the editor › Academic

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