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The couple and the psychotherapeutic group.
Kretsch RA, Benyakar M, Gurevitch M. Kretsch RA, et al. Among authors: gurevitch m. Isr J Psychiatry Relat Sci. 1995;32(3):184-93. Isr J Psychiatry Relat Sci. 1995. PMID: 8543459 Review.
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: gurevitch m. 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
Proximal 1q21 duplication: A syndrome or a susceptibility locus?
Levy M, Shohat M, Kahana S, Matar R, Klein K, Fishman IA, Gurevitch M, Basel-Salmon L, Maya I. Levy M, et al. Among authors: gurevitch m. Am J Med Genet A. 2023 Oct;191(10):2551-2557. doi: 10.1002/ajmg.a.63333. Epub 2023 Jun 26. Am J Med Genet A. 2023. PMID: 37357910
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: gurevitch m. Ultrasound Obstet Gynecol. 2023 Jun;61(6):698-704. doi: 10.1002/uog.26177. Ultrasound Obstet Gynecol. 2023. PMID: 36776119
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: gurevitch m. 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
17 results