Large scale population screening for Duchenne muscular dystrophy—Predictable and unpredictable challenges von Cohen, Gal, Shtorch‐Asor, Atalia, Ben‐Shachar, Shay, Goldfarb‐Yaacobi, Racheli, Kaiser, Meirav, Rosenfeld, Revital, Vinovezky, Mika, Irge, Dana, Furman, Yael, Reiss, Dafni, Litz‐Philipsborn, Shira, Sukenik‐Halevy, Rivka

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Prenatal diagnosis of a likely pathogenic variant in ZBTB18: Natural evolution of fetal phenotype including the long bones and corpus callosum von Birnbaum, Roee, Markovitch, Ofer, Biron‐shental, Tal, Kidron, Debora, Ben‐Sira, Liat, Litz Philipsborn, Shira, Reinstein, Eyal

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Recurring pathogenic variants in the BRCA2 gene in the Ethiopian Jewish population. Founder mutations? von Ludman, Mark D., Philipsborn, Shira Litz, Hartmajer, Shulamit, Shwartzman, Nitzan Sharon, Reinstein, Eyal

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Cancer risks in Jewish male BRCA1 and BRCA2 mutation carriers von Laitman, Yael, Keinan Boker, Lital, Liphsitz, Irena, Weissglas-Volkov, Daphna, Litz-Philipsborn, Shira, Schayek, Hagit, Friedman, Eitan

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Diagnostic yield of multigene panel testing in an Israeli cohort: enrichment of low-penetrance variants von Bernstein-Molho, Rinat, Friedman, Eitan, Kedar, Inbal, Laitman, Yael, Allweis, Tanir M., Gal-Yam, Einav Nili, Feldman, Hagit Baris, Grinshpun, Albert, Halpern, Naama, Hartmajer, Shulamit, Kadouri, Luna, Katz, Lior H., Kaufman, Bella, Laish, Ido, Levanon, Keren, Philipsborn, Shira Litz, Ludman, Mark, Moran, Gal, Peretz, Tamar, Reinstein, Eyal, Levi, Gili Reznick, Safra, Tamar, Shkedi, Shiri, Vinkler, Chana, Levy, Zohar, Goldberg, Yael

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A founder mutation in TCTN2 causes Meckel-Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin von Litz Philipsborn, Shira, Hartmajer, Shulamit, Shtorch Asor, Atalia, Vinovezky, Mika, Regev, Miriam, Singer, Amihood, Reinstein, Eyal

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A founder mutation in TCTN2 causes Meckel‐Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin von Litz Philipsborn, Shira, Hartmajer, Shulamit, Shtorch Asor, Atalia, Vinovezky, Mika, Regev, Miriam, Singer, Amihood, Reinstein, Eyal

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The impact of third-trimester genetic counseling von Sharony, Reuven, Engel, Offra, Litz-Philipsborn, Shira, Sukenik-Halevy, Rivka, Biron-Shental, Tal, Evans, Mark I.

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Prenatal diagnosis of a likely pathogenic variant in ZBTB18: Natural evolution of fetal phenotype including the long bones and corpus callosum von Birnbaum, Roee, Markovitch, Ofer, Biron-Shental, Tal, Kidron, Debora, Ben-Sira, Liat, Litz Philipsborn, Shira, Reinstein, Eyal

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