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Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing.
Johansson LF, de Boer EN, de Weerd HA, van Dijk F, Elferink MG, Schuring-Blom GH, Suijkerbuijk RF, Sinke RJ, Te Meerman GJ, Sijmons RH, Swertz MA, Sikkema-Raddatz B. Johansson LF, et al. Among authors: te meerman gj. Sci Rep. 2017 May 12;7(1):1838. doi: 10.1038/s41598-017-02031-5. Sci Rep. 2017. PMID: 28500333 Free PMC article.
Charles Buys (1942-2014).
Sijmons RH, te Meerman GJ, Hofstra RM. Sijmons RH, et al. Among authors: te meerman gj. Eur J Hum Genet. 2014 Dec;22(12):1343-4. doi: 10.1038/ejhg.2014.207. Eur J Hum Genet. 2014. PMID: 25393683 Free PMC article. No abstract available.
Probability tables for exclusion of mosaicism in prenatal diagnosis.
Sikkema-Raddatz B, Castedo S, Te Meerman GJ. Sikkema-Raddatz B, et al. Among authors: te meerman gj. Prenat Diagn. 1997 Feb;17(2):115-8. doi: 10.1002/(sici)1097-0223(199702)17:2<115::aid-pd37>3.0.co;2-a. Prenat Diagn. 1997. PMID: 9061758
No association between two MLH3 variants (S845G and P844L)and colorectal cancer risk.
de Jong MM, Hofstra RM, Kooi KA, Westra JL, Berends MJ, Wu Y, Hollema H, van der Sluis T, van der Graaf WT, de Vries EG, Schaapveld M, Sijmons RH, te Meerman GJ, Kleibeuker JH. de Jong MM, et al. Among authors: te meerman gj. Cancer Genet Cytogenet. 2004 Jul 1;152(1):70-1. doi: 10.1016/j.cancergencyto.2003.10.008. Cancer Genet Cytogenet. 2004. PMID: 15193445
Colorectal cancer and the CHEK2 1100delC mutation.
de Jong MM, Nolte IM, Te Meerman GJ, van der Graaf WT, Mulder MJ, van der Steege G, Bruinenberg M, Schaapveld M, Niessen RC, Berends MJ, Sijmons RH, Hofstra RM, de Vries EG, Kleibeuker JH. de Jong MM, et al. Among authors: te meerman gj. Genes Chromosomes Cancer. 2005 Aug;43(4):377-82. doi: 10.1002/gcc.20195. Genes Chromosomes Cancer. 2005. PMID: 15852425
144 results