Case report: Novel insights into hemorrhagic destruction of the brain, subependymal calcification, and cataracts disease by Tameemi Abdallah Moady, Marwan Odeh, Marwan Odeh, Ayalla Fedida, Zvi Segal, Zvi Segal, Maayan Gruber, Maayan Gruber, Moshe Goldfeld, Limor Kalfon, Tzipora C. Falik-Zaccai, Tzipora C. Falik-Zaccai

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A genetic survey of patients with familial idiopathic intracranial hypertension residing in a Middle Eastern village: genetic association study by Eran Berkowitz, Tzipora C. Falik Zaccai, Dana Irge, Inbar Gur, Beatrice Tiosano, Anat Kesler

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Challenges to effective and autonomous genetic testing and counseling for ethno-cultural minorities: a qualitative study by Nehama Cohen-Kfir, Miriam Ethel Bentwich, Andrew Kent, Nomy Dickman, Mary Tanus, Basem Higazi, Limor Kalfon, Mary Rudolf, Tzipora C. Falik-Zaccai

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Hereditary orotic aciduria identified by newborn screening by Orna Staretz-Chacham, Orna Staretz-Chacham, Orna Staretz-Chacham, Nadirah S. Damseh, Suha Daas, Nasser Abu Salah, Nasser Abu Salah, Yair Anikster, Yair Anikster, Ortal Barel, Elena Dumin, Elena Dumin, Aviva Fattal-Valevski, Aviva Fattal-Valevski, Tzipora C. Falik-Zaccai, Tzipora C. Falik-Zaccai, Eli Hershkovitz, Eli Hershkovitz, Eli Hershkovitz, Sagi Josefsberg, Yuval Landau, Yuval Landau, Tally Lerman-Sagie, Tally Lerman-Sagie, Hanna Mandel, Rachel Rock, Nira Rostami, Talya Saraf-Levy, Nava Shaul Lotan, Ronen Spiegel, Ronen Spiegel, Ronen Spiegel, Galit Tal, Galit Tal, Igor Ulanovsky, Yael Wilnai, Stanley H. Korman, Stanley H. Korman, Shlomo Almashanu

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Sequence variation in PPP1R13L results in a novel form of cardio‐cutaneous syndrome by Tzipora C Falik‐Zaccai, Yiftah Barsheshet, Hanna Mandel, Meital Segev, Avraham Lorber, Shachaf Gelberg, Limor Kalfon, Shani Ben Haroush, Adel Shalata, Liat Gelernter‐Yaniv, Sarah Chaim, Dorith Raviv Shay, Morad Khayat, Michal Werbner, Inbar Levi, Yishay Shoval, Galit Tal, Stavit Shalev, Eli Reuveni, Emily Avitan‐Hersh, Eugene Vlodavsky, Liat Appl‐Sarid, Dorit Goldsher, Reuven Bergman, Zvi Segal, Ora Bitterman‐Deutsch, Orly Avni

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Sequence variation in PPP1R13L results in a novel form of cardio‐cutaneous syndrome by Tzipora C Falik‐Zaccai, Yiftah Barsheshet, Hanna Mandel, Meital Segev, Avraham Lorber, Shachaf Gelberg, Limor Kalfon, Shani Ben Haroush, Adel Shalata, Liat Gelernter‐Yaniv, Sarah Chaim, Dorith Raviv Shay, Morad Khayat, Michal Werbner, Inbar Levi, Yishay Shoval, Galit Tal, Stavit Shalev, Eli Reuveni, Emily Avitan‐Hersh, Eugene Vlodavsky, Liat Appl‐Sarid, Dorit Goldsher, Reuven Bergman, Zvi Segal, Ora Bitterman‐Deutsch, Orly Avni

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