Nonmalignant Features Associated with Inherited Colorectal Cancer Syndromes-Clues for Diagnosis

por Haimov, Diana, Lieberman, Sari, Castellvi-Bel, Sergi, Nielsen, Maartje, Goldberg, Yael
Publicado 2022

Prenatal Isolated Ventricular Septal Defect May Not Be Associated with Trisomy 21

por Shen, Ori, Lieberman, Sari, Farber, Benjamin, Terner, Daniel, Lahad, Amnon, Levy-Lahad, Ephrat
Publicado 2014

Real World Cost-Effectiveness Analysis of Population Screening for BRCA Variants among Ashkenazi Jews Compared with Family History-Based Strategies

por Michaelson-Cohen, Rachel, Cohen, Matan J., Cohen, Carmit, Greenberg, Dan, Shmueli, Amir, Lieberman, Sari, Tomer, Ariela, Levy-Lahad, Ephrat, Lahad, Amnon
Publicado 2022

Variable Features of Juvenile Polyposis Syndrome With Gastric Involvement Among Patients With a Large Genomic Deletion of BMPR1A

por Lieberman, Sari, Beeri, Rachel, Walsh, Tom, Schechter, Menachem, Keret, Dan, Half, Elizabet, Gulsuner, Suleyman, Tomer, Ariela, Jacob, Harold, Cohen, Shlomi, Basel-Salmon, Lina, Mansur, Mahmud, Berger, Rachel, Katz, Lior H., Golomb, Eliahu, Peretz, Tamar, Levy, Zohar, Kedar, Inbal, King, Mary-Claire, Levy-Lahad, Ephrat, Goldberg, Yael
Publicado 2019

Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families

por Brownstein, Zippora, Friedman, Lilach M, Shahin, Hashem, Oron-Karni, Varda, Kol, Nitzan, Rayyan, Amal Abu, Parzefall, Thomas, Lev, Dorit, Shalev, Stavit, Frydman, Moshe, Davidov, Bella, Shohat, Mordechai, Rahile, Michele, Lieberman, Sari, Levy-Lahad, Ephrat, Lee, Ming K, Shomron, Noam, King, Mary-Claire, Walsh, Tom, Kanaan, Moien, Avraham, Karen B
Publicado 2011