1. Clinicians' attitudes towards parental choice in the era of advanced genomic tests in pregnancy. (19th July 2021) Authors: Macarov, Michal; Meiner, Vardiella; Chalk, Michal; Hochner, Hagit; Shkedi‐Rafid, Shiri Journal: Prenatal diagnosis Issue: Volume 41:Number 9(2021) Page Start: 1066 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Genetic counseling practice for inherited eye diseases in an Israeli medical center during the COVID‐19 pandemic. Issue 4 (19th July 2021) Authors: Macarov, Michal; Schneider, Nina; Eilat, Avital; Yahalom, Claudia Journal: Journal of genetic counseling Issue: Volume 30:Issue 4(2021) Page Start: 969 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Information Women Choose to Receive About Prenatal Chromosomal Microarray Analysis. Issue 1 (January 2020) Authors: Hochner, Hagit; Daum, Hagit; Douiev, Liza; Zvi, Naama; Frumkin, Ayala; Macarov, Michal; Kimchi-Shaal, Adva; Hacohen, Nuphar; Eilat, Avital; Faham, Duha; Shkedi-Rafid, Shiri Journal: Obstetrics and gynecology Issue: Volume 135:Issue 1(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Non‐confined long‐standing blood chimerism in a spontaneous monochorionic dizygotic twin pregnancy. Issue 3 (26th November 2019) Authors: Daum, Hagit; Frumkin, Ayala; Meiner, Vardiella; Werner, Marion; Macarov, Michal; Gillis, David; Israel, Shoshana; Abed El Latif, Mahmoud; Meir, Karen; Gielchinsky, Yuval Journal: International journal of gynaecology and obstetrics Issue: Volume 148:Issue 3(2020) Page Start: 399 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Postpartum women's attitudes to disclosure of adult‐onset conditions in pregnancy. (4th May 2022) Authors: Libman, Vitalia; Macarov, Michal; Friedlander, Yechiel; Goldman‐Mellor, Sidra; Israel, Salomon; Hochner‐Celnikier, Drorith; Sompolinsky, Yishai; Dior, Uri Pinchas; Osovsky, Michael; Basel‐Salmon, Lina; Wiznitzer, Arnon; Neumark, Yehuda; Meiner, Vardiella; Frumkin, Ayala; Shkedi‐Rafid, Shiri; Hoch... Journal: Prenatal diagnosis Issue: Volume 42:Number 8(2022) Page Start: 1038 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Preimplantation genetic diagnosis as a strategy to prevent having a child born with an heritable eye disease. (4th July 2018) Authors: Yahalom, Claudia; Macarov, Michal; Lazer-Derbeko, Galit; Altarescu, Gheona; Imbar, Tal; Hyman, Jordana H.; Eldar-Geva, Talia; Blumenfeld, Anat Journal: Ophthalmic genetics Issue: Volume 39:Number 4(2018) Page Start: 450 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. SENIOR–LØKEN SYNDROME: A Case Series and Review of the Renoretinal Phenotype and Advances of Molecular Diagnosis. Issue 10 (October 2021) Authors: Yahalom, Claudia; Volovelsky, Oded; Macarov, Michal; Altalbishi, Alaa; Alsweiti, Yahya; Schneider, Nina; Hanany, Mor; Khan, Muhammad Imran; Cremers, Frans P.M.; Anteby, Irene; Banin, Eyal; Sharon, Dror; Khateb, Samer Journal: Retina Issue: Volume 41:Issue 10(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1. Issue 4 (24th August 2020) Authors: Brownstein, Zippora; Gulsuner, Suleyman; Walsh, Tom; Martins, Fábio T.A.; Taiber, Shahar; Isakov, Ofer; Lee, Ming K.; Bordeynik‐Cohen, Mor; Birkan, Maria; Chang, Weise; Casadei, Silvia; Danial‐Farran, Nada; Abu‐Rayyan, Amal; Carlson, Ryan; Kamal, Lara; Arnthórsson, Asgeir Ö.; Sokolov, Meirav; Gil... Journal: Clinical genetics Issue: Volume 98:Issue 4(2020) Page Start: 353 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children. Issue 6 (November 2021) Authors: Levinger, Nadav; Hendler, Karen; Banin, Eyal; Hanany, Mor; Kimchi, Adva; Mechoulam, Hadas; Meiner, Vardiella; Parag, Yoav; Sharon, Dror; Macarov, Michal; Yahalom, Claudia Journal: European journal of ophthalmology Issue: Volume 31:Issue 6(2021) Page Start: 3349 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗