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Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.
Sagi-Dain L, Cohen Vig L, Kahana S, Yacobson S, Tenne T, Agmon-Fishman I, Klein C, Matar R, Basel-Salmon L, Maya I. Sagi-Dain L, et al. Among authors: klein c. Genet Med. 2019 Nov;21(11):2462-2467. doi: 10.1038/s41436-019-0550-x. Epub 2019 May 24. Genet Med. 2019. PMID: 31123319 Free article.
Residual risk for clinically significant copy number variants in low-risk pregnancies, following exclusion of noninvasive prenatal screening-detectable findings.
Maya I, Salzer Sheelo L, Brabbing-Goldstein D, Matar R, Kahana S, Agmon-Fishman I, Klein C, Gurevitch M, Basel-Salmon L, Sagi-Dain L. Maya I, et al. Among authors: klein c. Am J Obstet Gynecol. 2022 Apr;226(4):562.e1-562.e8. doi: 10.1016/j.ajog.2021.11.016. Epub 2021 Nov 8. Am J Obstet Gynecol. 2022. PMID: 34762861
Clinical utility of expanded non-invasive prenatal screening compared with chromosomal microarray analysis in over 8000 pregnancies without major structural anomaly.
Maya I, Salzer Sheelo L, Brabbing-Goldstein D, Matar R, Kahana S, Agmon-Fishman I, Klein C, Gurevitch M, Basel-Salmon L, Sagi-Dain L. Maya I, et al. Among authors: klein c. Ultrasound Obstet Gynecol. 2023 Jun;61(6):698-704. doi: 10.1002/uog.26177. Ultrasound Obstet Gynecol. 2023. PMID: 36776119 Free article.
Prevalence of high-penetrant copy number variants in 7734 low-risk pregnancies.
Sagi-Dain L, Salzer Sheelo L, Brabbing-Goldstein D, Matar R, Kahana S, Agmon-Fishman I, Klein C, Gurevitch M, Basel-Salmon L, Maya I. Sagi-Dain L, et al. Among authors: klein c. Am J Obstet Gynecol MFM. 2023 Dec;5(12):101201. doi: 10.1016/j.ajogmf.2023.101201. Epub 2023 Oct 21. Am J Obstet Gynecol MFM. 2023. PMID: 37871696
4,050 results