Rezultati - Sagi, Michal

Cancer risks in carriers of the BRCA1/2 Ashkenazi founder mutations od Kadouri, Luna, Hubert, Ayala, Rotenberg, Yakir, Hamburger, Tamar, Sagi, Michal, Nechushtan, Chovav, Abeliovich, Dvorah, Peretz, Tamar

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‘My funky genetics’: BRCA1/2 mutation carriers’ understanding of genetic inheritance and reproductive merger in the context of new repro-genetic technologies od Werner-Lin, Allison, Rubin, Lisa R., Doyle, Maya, Stern, Rikki, Savin, Katie, Hurley, Karen, Sagi, Michal

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Incorporating information about pre-implantation genetic diagnosis into discussions about testing and risk-management for BRCA1/2 mutations: A qualitative study of patient preferen... od Hurley, Karen, Rubin, Lisa, Werner-Lin, Allison, Sagi, Michal, Kemel, Yelena, Stern, Rikki, Phillips, Aliza, Cholst, Ina, Kauff, Noah, Offit, Kenneth

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A novel BRCA-1 mutation in Arab kindred from east Jerusalem with breast and ovarian cancer od Kadouri, Luna, Bercovich, Dani, Elimelech, Arava, Lerer, Israela, Sagi, Michal, Glusman, Gila, Shochat, Chen, Korem, Sigal, Hamburger, Tamar, Nissan, Aviram, Abu-Halaf, Nahil, Badrriyah, Muhmud, Abeliovich, Dvorah, Peretz, Tamar

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Genome-wide SNP Genotyping Identifies the Stereocilin (STRC) Gene as a Major Contributor to Pediatric Bilateral Sensorineural Hearing Impairment od Francey, Lauren J, Conlin, Laura K, Kadesch, Hanna E, Clark, Dinah, Berrodin, Donna, Sun, Yi, Glessner, Joe, Hakonarson, Hakon, Jalas, Chaim, Landau, Chaim, Spinner, Nancy B, Kenna, Margaret, Sagi, Michal, Rehm, Heidi L, Krantz, Ian D

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Further localization of X-linked hydrocephalus in the chromosomal region Xq28 od Willems, Patrick J., Vits, Lieve, Raeymaekers, Peter, Beuten, Joke, Coucke, Paul, Holden, Jeanette J. A., Van Broeckhoven, Christine, Warren, Stephen T., Sagi, Michal, Robinson, David, Dennis, Nick, Friedman, Kenneth J., Magnay, Dorothy, Lyonnet, Stanislas, White, Bradley N., Wittwer, Bärbel H., Aylsworth, Arthur S., Reicke, Sigrid

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Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies od Beryozkin, Avigail, Shevah, Elia, Kimchi, Adva, Mizrahi-Meissonnier, Liliana, Khateb, Samer, Ratnapriya, Rinki, Lazar, Csilla H., Blumenfeld, Anat, Ben-Yosef, Tamar, Hemo, Yitzhak, Pe’er, Jacob, Averbuch, Eduard, Sagi, Michal, Boleda, Alexis, Gieser, Linn, Zlotogorski, Abraham, Falik-Zaccai, Tzipora, Alimi-Kasem, Ola, Jacobson, Samuel G., Chowers, Itay, Swaroop, Anand, Banin, Eyal, Sharon, Dror

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Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1 od Brownstein, Zippora, Gulsuner, Suleyman, Walsh, Tom, Martins, Fábio Tadeu Arrojo, Taiber, Shahar, Isakov, Ofer, Lee, Ming K., Bordeynik-Cohen, Mor, Birkan, Maria, Chang, Weise, Casadei, Silvia, Danial-Farran, Nada, Abu-Rayyan, Amal, Carlson, Ryan, Kamal, Lara, Arnþórsson, Ásgeir Örn, Sokolov, Meirav, Gilony, Dror, Lipschitz, Noga, Frydman, Moshe, Davidov, Bella, Macarov, Michal, Sagi, Michal, Vinkler, Chana, Poran, Hana, Sharony, Reuven, Samara, Nadra, Zvi, Na’ama, Baris-Feldman, Hagit, Singer, Amihood, Handzel, Ophir, Hertzano, Ronna, Ali-Naffaa, Doaa, Ruhrman-Shahar, Noa, Madgar, Ory, Sofrin, Efrat, Peleg, Amir, Khayat, Morad, Shohat, Mordechai, Basel-Salmon, Lina, Pras, Elon, Lev, Dorit, Wolf, Michael, Steingrimsson, Eirikur, Shomron, Noam, Kelley, Matthew W., Kanaan, Moien, Allon-Shalev, Stavit, King, Mary-Claire, Avraham, Karen B.

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