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78 results

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Page 1
Whole-genome array as a first-line cytogenetic test in prenatal diagnosis.
Srebniak MI, Van Opstal D, Joosten M, Diderich KE, de Vries FA, Riedijk S, Knapen MF, Go AT, Govaerts LC, Galjaard RJ. Srebniak MI, et al. Ultrasound Obstet Gynecol. 2015 Apr;45(4):363-72. doi: 10.1002/uog.14745. Ultrasound Obstet Gynecol. 2015. PMID: 25488734 Free article. No abstract available.
Prenatal and postnatal findings in small-for-gestational-age fetuses without structural ultrasound anomalies at 18-24 weeks.
de Wit MC, Srebniak MI, Joosten M, Govaerts LC, Kornelisse RF, Papatsonis DN, de Graaff K, Knapen MF, Bruggenwirth HT, de Vries FA, Van Veen S, Van Opstal D, Galjaard RJ, Go AT. de Wit MC, et al. Ultrasound Obstet Gynecol. 2017 Mar;49(3):342-348. doi: 10.1002/uog.15949. Ultrasound Obstet Gynecol. 2017. PMID: 27102944 Free article.
Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?
van der Steen SL, Bunnik EM, Polak MG, Diderich KEM, Verhagen-Visser J, Govaerts LCP, Joosten M, Knapen MFCM, Go ATJI, Van Opstal D, Srebniak MI, Galjaard RJH, Tibben A, Riedijk SR. van der Steen SL, et al. Among authors: galjaard rjh. J Genet Couns. 2018 Feb;27(1):85-94. doi: 10.1007/s10897-017-0124-5. Epub 2017 Jul 4. J Genet Couns. 2018. PMID: 28674770 Free PMC article.
Prenatal cell-free DNA testing of women with pregnancy-associated cancer: a retrospective cross-sectional study.
Heesterbeek CJ, Tjan-Heijnen VCG, Heimovaara JH, Lenaerts L, Lok C, Vriens IJH, Van Opstal D, Boon EMJ, Sie D, de Die-Smulders CEM, Amant F, Macville MVE; Dutch NIPT Consortium. Heesterbeek CJ, et al. Lancet Reg Health Eur. 2024 Aug 7;45:101024. doi: 10.1016/j.lanepe.2024.101024. eCollection 2024 Oct. Lancet Reg Health Eur. 2024. PMID: 39220433 Free PMC article.
[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.
Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: two patients and review of the literature.
Klaassens M, Galjaard RJ, Scott DA, Brüggenwirth HT, van Opstal D, Fox MV, Higgins RR, Cohen-Overbeek TE, Schoonderwaldt EM, Lee B, Tibboel D, de Klein A. Klaassens M, et al. Am J Med Genet A. 2007 Sep 15;143A(18):2204-12. doi: 10.1002/ajmg.a.31892. Am J Med Genet A. 2007. PMID: 17702015 Review.
78 results