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Page 1
Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up Study.
Heesterbeek CJ, Aukema SM, Galjaard RH, Boon EMJ, Srebniak MI, Bouman K, Faas BHW, Govaerts LCP, Hoffer MJV, den Hollander NS, Lichtenbelt KD, van Maarle MC, van Prooyen Schuurman L, van Rij MC, Schuring-Blom GH, Stevens SJC, Tan-Sindhunata G, Zamani Esteki M, de Die-Smulders CEM, Tjan-Heijnen VCG, Henneman L, Sistermans EA, Macville MVE; Dutch NIPT Consortium. Heesterbeek CJ, et al. Among authors: schuring blom gh. J Clin Oncol. 2022 Aug 1;40(22):2426-2435. doi: 10.1200/JCO.21.02260. Epub 2022 Apr 8. J Clin Oncol. 2022. PMID: 35394817
[Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities].
Boormans EM, van Lith JM, Bilardo CM, Knegt AC, Oepkes D, Hoffer MJ, Boon EM, Wildschut HI, Galjaard RJ, Schuring-Blom GH, van Oppen AC, Smits A, Creemers J, Go A, Nieuwint A, Nijhuis JG, de Die C, Bonsel GJ, Birnie E, Leschot N. Boormans EM, et al. Ned Tijdschr Geneeskd. 2006 Nov 4;150(44):2455; author reply 2455. Ned Tijdschr Geneeskd. 2006. PMID: 17131707 Dutch. No abstract available.
From karyotyping to array-CGH in prenatal diagnosis.
Lichtenbelt KD, Knoers NV, Schuring-Blom GH. Lichtenbelt KD, et al. Among authors: schuring blom gh. Cytogenet Genome Res. 2011;135(3-4):241-50. doi: 10.1159/000334065. Epub 2011 Nov 12. Cytogenet Genome Res. 2011. PMID: 22086062 Review.
Unexplained False Negative Results in Noninvasive Prenatal Testing: Two Cases Involving Trisomies 13 and 18.
Hochstenbach R, Page-Christiaens GC, van Oppen AC, Lichtenbelt KD, van Harssel JJ, Brouwer T, Manten GT, van Zon P, Elferink M, Kusters K, Akkermans O, Ploos van Amstel JK, Schuring-Blom GH. Hochstenbach R, et al. Among authors: schuring blom gh. Case Rep Genet. 2015;2015:926545. doi: 10.1155/2015/926545. Epub 2015 Jun 7. Case Rep Genet. 2015. PMID: 26137330 Free PMC article.
29 results