1. Chromosomal Microarray Analysis Compared With Noninvasive Prenatal Testing in Pregnancies With Abnormal Maternal Serum Screening. Issue 5 (5th May 2022) Authors: Sagi-Dain, Lena; Salzer Sheelo, Liat; Brabbing-Goldstein, Dana; Matar, Reut; Kahana, Sarit; Agmon-Fishman, Ifaat; Klein, Cochava; Gurevitch, Merav; Basel-Salmon, Lina; Maya, Idit Journal: Obstetrics and gynecology Issue: Volume 139:Issue 5(2022) Page Start: 877 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Chromosomal Microarray vs. NIPS: Analysis of 5541 Low-Risk Pregnancies. Issue 4 (April 2020) Authors: Sagi-Dain, Lena; Vig, Lital Cohen; Kahana, Sarit; Yacobson, Shiri; Tenne, Tamar; Agmon-Fishman, Ifat; Klein, Cochava; Matar, Reut; Basel-Salmon, Lina; Maya, Idit Journal: Obstetrical & gynecological survey Issue: Volume 75:Issue 4(2020) Page Start: 222 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Chromosomal Microarray vs. NIPS: Analysis of 5541 Low-Risk Pregnancies. Issue 4 (April 2020) Authors: Sagi-Dain, Lena; Vig, Lital Cohen; Kahana, Sarit; Yacobson, Shiri; Tenne, Tamar; Agmon-Fishman, Ifat; Klein, Cochava; Matar, Reut; Basel-Salmon, Lina; Maya, Idit Journal: Obstetrical & gynecological survey Issue: Volume 75:Issue 4(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Residual Risk for Clinically Significant Copy Number Variants in Low-Risk Pregnancies, Following Exclusion of Noninvasive Prenatal Screening–Detectable Findings. Issue 10 (October 2022) Authors: Maya, Idit; Sheelo, Liat Salzer; Brabbing-Goldstein, Dana; Matar, Reut; Kahana, Sarit; Agmon-Fishman, Ifaat; Klein, Cochava; Gurevitch, Merav; Basel-Salmon, Lina; Sagi-Dain, Lena Journal: Obstetrical & gynecological survey Issue: Volume 77:Issue 10(2022) Page Start: 574 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. The phenotype of 15 cases with rare 8q24.13‐q24.3 deletions–A new syndrome or still an enigma?. Issue 5 (22nd February 2021) Authors: Maya, Idit; Kahana, Sarit; Agmon‐Fishman, Ifaat; Klein, Cochava; Matar, Reut; Berger, Racheli; Josefsberg, Sagi Ben Yehoshua; Shohat, Mordechai; Marom, Daphna; Basel‐Salmon, Lina; Sagi‐Dain, Lena Journal: American journal of medical genetics Issue: Volume 185:Issue 5(2021) Page Start: 1461 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗