1. Abnormal nuchal translucency followed by normal microarray analysis is associated with placental pathology‐related complications. (25th January 2021) Authors: Krispin, Eyal; Kushnir, Anya; Shemer, Asaf; Rienstein, Shlomit; Berkenstadt, Michal; Yinon, Yoav; Weisz, Boaz Journal: Prenatal diagnosis Issue: Volume 41:Number 7(2021) Page Start: 855 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Chromosomal Microarray Analysis in Pregnancies With Corpus Callosum or Posterior Fossa Anomalies. (June 2021) Authors: Greenbaum, Lior; Maya, Idit; Sagi-Dain, Lena; Sukenik-Halevy, Rivka; Berkenstadt, Michal; Yonath, Hagith; Rienstein, Shlomit; Shalata, Adel; Katorza, Eldad; Singer, Amihood Journal: Neurology Issue: Volume 7:Number 3(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Fetal pleural effusion: Contemporary methods of genetic evaluation. (16th July 2019) Authors: Weissbach, Tal; Kushnir, Anya; Rasslan, Rana; Rosenblatt, Orgad; Yinon, Yoav; Berkenstadt, Michal; Weisz, Boaz; Mazaki Tovi, Shali; Kassif, Eran Journal: Prenatal diagnosis Issue: Volume 39:Number 9(2019) Page Start: 751 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. LMOD3‐Associated Nemaline Myopathy: Prenatal Ultrasonographic, Pathologic, and Molecular Findings. (13th January 2018) Authors: Berkenstadt, Michal; Pode‐Shakked, Ben; Barel, Ortal; Barash, Hila; Achiron, Reuven; Gilboa, Yinon; Kidron, Dvora; Raas‐Rothschild, Annick Journal: Journal of ultrasound in medicine Issue: Volume 37:Number 7(2018) Page Start: 1827 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Neurodevelopmental outcome following prenatal diagnosis of a short corpus callosum. (26th April 2019) Authors: Meidan, Roni; Bar‐Yosef, Omer; Ashkenazi, Itay; Yahal, Orr; Berkenstadt, Michal; Hoffman, Chen; Tsur, Abraham; Achiron, Reuven; Katorza, Eldad Journal: Prenatal diagnosis Issue: Volume 39:Number 6(2019) Page Start: 477 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Nonobstructive Diffuse Dilated Bowel Loops: Prenatal Diagnosis, Fetal Characteristics and Neonatal Outcomes. (8th December 2016) Authors: Katz, Guy; Pode‐Shakked, Ben; Berkenstadt, Michal; Bilik, Ron; Polak Charcon, Sylvie; Barshack, Iris; Achiron, Reuven; Gilboa, Yinon Journal: Journal of ultrasound in medicine Issue: Volume 36:Number 1(2017) Page Start: 149 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Patients' Attitudes Towards Disclosure of Genetic Test Results to Family Members: The Impact of Patients' Sociodemographic Background and Counseling Experience. Issue 2 (14th September 2015) Authors: Gilbar, Roy; Shalev, Stavit; Spiegel, Ronen; Pras, Elon; Berkenstadt, Michal; Sagi, Michal; Ben‐Yehuda, Adi; Mor, Pnina; Perry, Shlomit; Zaccai, Tzipora Falik; Borochowitz, Zvi; Barnoy, Sivia Journal: Journal of genetic counseling Issue: Volume 25:Issue 2(2016) Page Start: 314 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Prenatal abnormal width of the cavum septum pellucidum – MRI features and neurodevelopmental outcome. (17th November 2018) Authors: Cooper, Shiri; Katorza, Eldad; Berkenstadt, Michal; Hoffmann, Chen; Achiron, Reuven; Bar-Yosef, Omer Journal: Journal of maternal-fetal & neonatal medicine Issue: Volume 31:Number 22(2018) Page Start: 3043 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Prenatal diagnosis for de novo mutations: Experience from a tertiary center over a 10‐year period. Issue 4 (28th January 2019) Authors: Eyal, Ori; Berkenstadt, Michal; Reznik‐Wolf, Haike; Poran, Hana; Ziv‐Baran, Tomer; Greenbaum, Lior; Yonath, Hagit; Pras, Elon Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 4(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Prenatal diagnosis of 17q12 deletion syndrome: from fetal hyperechogenic kidneys to high risk for autism. (25th October 2016) Authors: Gilboa, Yinon; Perlman, Sharon; Pode‐Shakked, Naomi; Pode‐Shakked, Ben; Shrim, Alon; Azaria‐Lahav, Einat; Dekel, Benjamin; Yonath, Hagith; Berkenstadt, Michal; Achiron, Reuven Journal: Prenatal diagnosis Issue: Volume 36:Number 11(2016) Page Start: 1027 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗