1. Ameloblastic Fibroodontoma of the Mandible with Normal Karyotype in a Pediatric Patient. (9th August 2012) Authors: Manor, Esther; Kan, Elena; Bodner, Lipa Other Names: Darling M. Academic Editor.; Varela-Centelles P. I. Academic Editor. Journal: Case reports in dentistry Issue: Volume 2012(2012) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Can bone marrow cellularity help in predicting prognosis in myelodysplastic syndromes?. (31st August 2018) Authors: Greenbaum, Uri; Joffe, Erel; Filanovsky, Kalman; Oster, Howard S.; Kirgner, Ilya; Levi, Itai; Raanani, Pia; Avivi, Irit; Manor, Esther; Man‐El, Gili; Mittelman, Moshe Journal: European journal of haematology Issue: Volume 101:Number 4(2018) Page Start: 502 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies. Issue 6 (December 2018) Authors: Sagi-Dain, Lena; Maya, Idit; Reches, Adi; Frumkin, Ayala; Grinshpun-Cohen, Julia; Segel, Reeval; Manor, Esther; Khayat, Morad; Tenne, Tamar; Banne, Ehud; Shalata, Adel; Yonath, Hagith; Berger, Racheli; Singer, Amihood; Ben-Shachar, Shay Journal: Obstetrics and gynecology Issue: Volume 132:Issue 6(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Clonal evolution through genetic bottlenecks and telomere attrition: Potential threats to in vitro data reproducibility. Issue 7 (29th November 2018) Authors: Gisselsson, David; Lichtenzstejn, Daniel; Kachko, Polina; Karlsson, Jenny; Manor, Esther; Mai, Sabine Other Names: Mai Sabine guestEditor. Journal: Genes, chromosomes & cancer Issue: Volume 58:Issue 7(2019) Page Start: 452 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribe. Issue 12 (4th December 2018) Authors: Wormser, Ohad; Gradstein, Libe; Kadar, Einat; Yogev, Yuval; Perez, Yonatan; Mashkit, Elena; Elbedour, Khalil; Drabkin, Max; Markus, Barak; Kadir, Rotem; Halperin, Daniel; Khalaila, Soltan; Levy, Jaime; Lifshitz, Tova; Manor, Esther; Birk, Ohad S. Journal: American journal of medical genetics Issue: Volume 176:Issue 12(2018) Page Start: 2695 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Oral Mucoceles in Children—Analysis of 56 New Cases. Issue 5 (6th April 2015) Authors: Bodner, Lipa; Manor, Esther; Joshua, Ben‐Zion; Shaco‐Levy, Ruthy Journal: Pediatric dermatology Issue: Volume 32:Issue 5(2015) Page Start: 647 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. The role of AGG interruptions in the FMR1 gene stability: A survey in ethnic groups with low and high rate of consanguinity. Issue 10 (27th August 2019) Authors: Manor, Esther; Gonen, Raphael; Sarussi, Benjamin; Keidar‐Friedman, Danielle; Kumar, Jay; Tang, Hiu‐Tung; Tassone, Flora Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 10(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. TMEM70 deficiency: Novel mutation and hypercitrullinemia during metabolic decompensation. Issue 7 (4th April 2019) Authors: Staretz‐Chacham, Orna; Wormser, Ohad; Manor, Esther; Birk, Ohad S.; Ferreira, Carlos R. Journal: American journal of medical genetics Issue: Volume 179:Issue 7(2019) Page Start: 1293 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗