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The following term was not found in PubMed: Kyriaki-Nefeli
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Fifteen-minute consultation: congenital nasolacrimal duct obstruction.
Mataftsi A, Malamaki P, Tsinopoulos IT, Symeonidis C, Dimitrakos SA, Ziakas N. Mataftsi A, et al. Arch Dis Child Educ Pract Ed. 2014 Apr;99(2):42-7. doi: 10.1136/archdischild-2012-303417. Epub 2013 Sep 23. Arch Dis Child Educ Pract Ed. 2014. PMID: 24063861 Review. No abstract available.
De novo Unbalanced 1;22 Translocation with 22q11 Deletion Syndrome.
Vittas S, Efstathiou G, Tsakalidis C, Malamaki C, Antari V, Chatzitoliou E, Chatziioannidis I, Galli-Tsinopoulou A, Soubasi V. Vittas S, et al. Cytogenet Genome Res. 2019;158(1):32-37. doi: 10.1159/000497173. Epub 2019 Feb 16. Cytogenet Genome Res. 2019. PMID: 30799418
IOP measurement: importance of methodology.
Mataftsi A, Malamaki P, Kappos N. Mataftsi A, et al. Int Ophthalmol. 2015 Oct;35(5):617. doi: 10.1007/s10792-015-0090-6. Epub 2015 Jun 2. Int Ophthalmol. 2015. PMID: 26031791 No abstract available.
Dual testing with QF-PCR and karyotype analysis for prenatal diagnosis of chromosomal abnormalities. Evaluation of 13,500 cases with consideration of using QF-PCR as a stand-alone test according to referral indications.
Papoulidis I, Siomou E, Sotiriadis A, Efstathiou G, Psara A, Sevastopoulou E, Anastasakis E, Sifakis S, Tsiligianni T, Kontodiou M, Malamaki C, Tzimina M, Petersen MB, Manolakos E, Athanasiadis A. Papoulidis I, et al. Prenat Diagn. 2012 Jul;32(7):680-5. doi: 10.1002/pd.3888. Epub 2012 Apr 18. Prenat Diagn. 2012. PMID: 22513450