Researcher

Paulussen, A.D.C.

Scientific laboratory officer

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  1. 2019
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  4. 2018
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  11. 2017
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  18. 2016
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    Putoux, A., Alqahtani, A., Pinson, L., Paulussen, A. D. C., Michel, J., Besson, A., ... Edery, P. (2016). Refining the phenotypical and mutational spectrum of Taybi-Linder syndrome. Clinical Genetics, 90(6), 550-555. https://doi.org/10.1111/cge.12781
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  24. 2015
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    Mersy, E., Faas, B. H. W., Spierts, S., Houben, L. M. H., Macville, M. V. E., Frints, S. G. M., ... Veltman, J. A. (2015). Cell-Free RNA Is a Reliable Fetoplacental Marker in Noninvasive Fetal Sex Determination. Clinical Chemistry, 61(12), 1515-1523. https://doi.org/10.1373/clinchem.2015.244962
  26. 2014
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    Natesan, S. A., Bladon, A. J., Coskun, S., Qubbaj, W., Prates, R., Munne, S., ... Handyside, A. H. (2014). Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro. Genetics in Medicine, 16(11), 838-845. https://doi.org/10.1038/gim.2014.45
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  29. 2013
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  32. 2012
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    Solomon, B. D., Bear, K. A., Wyllie, A., Keaton, A. A., Dubourg, C., David, V., ... Muenke, M. (2012). Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog. Journal of Medical Genetics, 49(7), 473-479. https://doi.org/10.1136/jmedgenet-2012-101008
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  38. 2011
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    Paulussen, A. D. C., Stegmann, A. P. A., Blok, M. J., Tserpelis, D., Posma-Velter, C., Detisch, Y., ... Schrander-Stumpel, C. T. R. M. (2011). MLL2 Mutation Spectrum in 45 Patients with Kabuki Syndrome. Human Mutation, 32(2), E2018-E2025. https://doi.org/10.1002/humu.21416
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  42. 2010
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  46. 2009
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  48. 2008
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  53. 2007
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  56. 2006
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  59. 2005
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  64. 2004
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