Risultati della ricerca - Abeliovich, Dvorah

The 28-kb Deletion Spanning D15S63 Is a Polymorphic Variant in the Ashkenazi Jewish Population di Silverstein, Shira, Lerer, Israela, Buiting, Karin, Abeliovich, Dvorah

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

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The H Syndrome Is Caused by Mutations in the Nucleoside Transporter hENT3 di Molho-Pessach, Vered, Lerer, Israela, Abeliovich, Dvorah, Agha, Ziad, Abu Libdeh, Abdulasalam, Broshtilova, Valentina, Elpeleg, Orly, Zlotogorski, Abraham

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A 28-kb Deletion Spanning D15S63 (PW71) in Five Families: A Rare Neutral Variant? di Buiting, Karin, Dittrich, Bärbel, Dworniczak, Bernd, Lerer, Israela, Abeliovich, Dvorah, Cottrell, Sally, Temple, I. Karen, Harvey, John F., Lich, Christina, Groß, Stephanie, Horsthemke, Bernhard

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A novel BRCA-1 mutation in Arab kindred from east Jerusalem with breast and ovarian cancer di 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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Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study di del Castillo, Ignacio, Moreno-Pelayo, Miguel A., del Castillo, Francisco J., Brownstein, Zippora, Marlin, Sandrine, Adina, Quint, Cockburn, David J., Pandya, Arti, Siemering, Kirby R., Chamberlin, G. Parker, Ballana, Ester, Wuyts, Wim, Maciel-Guerra, Andréa Trevas, Álvarez, Araceli, Villamar, Manuela, Shohat, Mordechai, Abeliovich, Dvorah, Dahl, Hans-Henrik M., Estivill, Xavier, Gasparini, Paolo, Hutchin, Tim, Nance, Walter E., Sartorato, Edi L., Smith, Richard J. H., Van Camp, Guy, Avraham, Karen B., Petit, Christine, Moreno, Felipe

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