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• Recurrent benign copy number variants & issues in interpretation of variants of unknown significance identified by cytogenetic microarray in Indian patients with intellectual disability.

  Boggula VR, Agarwal M, Kumar R, Awasthi S, Phadke SR. Boggula VR, et al. Indian J Med Res. 2015 Dec;142(6):699-712. doi: 10.4103/0971-5916.174561. Indian J Med Res. 2015. PMID: 26831419 Free PMC article.
• The scope of prenatal diagnosis for women at increased risk for aneuploidies: views and preferences of professionals and potential users.

  de Jong A, Dondorp WJ, Krumeich A, Boonekamp J, van Lith JM, de Wert GM. de Jong A, et al. J Community Genet. 2013 Jan;4(1):125-35. doi: 10.1007/s12687-012-0126-9. Epub 2012 Nov 9. J Community Genet. 2013. PMID: 23138342 Free PMC article.
• Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH.

  Manolakos E, Kefalas K, Vetro A, Oikonomidou E, Daskalakis G, Psara N, Siomou E, Papageorgiou E, Sevastopoulou E, Konstantinidou A, Vrachnis N, Thomaidis L, Zuffardi O, Papoulidis I. Manolakos E, et al. Mol Cytogenet. 2013 Oct 31;6(1):47. doi: 10.1186/1755-8166-6-47. Mol Cytogenet. 2013. PMID: 24176130 Free PMC article.
• Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.

  Fiorentino F, Napoletano S, Caiazzo F, Sessa M, Bono S, Spizzichino L, Gordon A, Nuccitelli A, Rizzo G, Baldi M. Fiorentino F, et al. Eur J Hum Genet. 2013 Jul;21(7):725-30. doi: 10.1038/ejhg.2012.253. Epub 2012 Dec 5. Eur J Hum Genet. 2013. PMID: 23211699 Free PMC article.
• Spontaneous abortion and recurrent miscarriage: A comparison of cytogenetic diagnosis in 250 cases.

  Choi TY, Lee HM, Park WK, Jeong SY, Moon HS. Choi TY, et al. Obstet Gynecol Sci. 2014 Nov;57(6):518-25. doi: 10.5468/ogs.2014.57.6.518. Epub 2014 Nov 20. Obstet Gynecol Sci. 2014. PMID: 25469342 Free PMC article.