Diagnostic yield of multigene panel testing in an Israeli cohort: enrichment of low-penetrance variants
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
Published in Breast cancer research and treatment (01.06.2020)
Published in Breast cancer research and treatment (01.06.2020)
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A founder mutation in TCTN2 causes Meckel-Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin
Litz Philipsborn, Shira, Hartmajer, Shulamit, Shtorch Asor, Atalia, Vinovezky, Mika, Regev, Miriam, Singer, Amihood, Reinstein, Eyal
Published in American journal of medical genetics. Part A (01.05.2021)
Published in American journal of medical genetics. Part A (01.05.2021)
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Journal Article
A founder mutation in TCTN2 causes Meckel‐Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin
Litz Philipsborn, Shira, Hartmajer, Shulamit, Shtorch Asor, Atalia, Vinovezky, Mika, Regev, Miriam, Singer, Amihood, Reinstein, Eyal
Published in American journal of medical genetics. Part A (01.05.2021)
Published in American journal of medical genetics. Part A (01.05.2021)
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The yield of full BRCA1/2 genotyping in Israeli high-risk breast/ovarian cancer patients who do not carry the predominant mutations
Barnes-Kedar, Inbal, Bernstein-Molho, Rinat, Ginzach, Nava, Hartmajer, Shulamit, Shapira, Tamar, Magal, Nurit, Kalis, Marina Lifshitc, Peretz, Tamar, Shohat, Mordechai, Basel-Salmon, Lina, Friedman, Eitan, Bazak, Lily, Goldberg, Yael
Published in Breast cancer research and treatment (01.11.2018)
Published in Breast cancer research and treatment (01.11.2018)
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