檢索結果 - Lerer, Israela

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  1. 1
    The 28-kb Deletion Spanning D15S63 Is a Polymorphic Variant in the Ashkenazi Jewish Population

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

    出版 2001
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  2. 2
    The H Syndrome Is Caused by Mutations in the Nucleoside Transporter hENT3

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

    出版 2008
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  3. 3
    Mutations of the Mitochondrial Holocytochrome c–Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome

    Mutations of the Mitochondrial Holocytochrome c–Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome 由 Wimplinger, Isabella, Morleo, Manuela, Rosenberger, Georg, Iaconis, Daniela, Orth, Ulrike, Meinecke, Peter, Lerer, Israela, Ballabio, Andrea, Gal, Andreas, Franco, Brunella, Kutsche, Kerstin

    出版 2006
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  4. 4
    A 28-kb Deletion Spanning D15S63 (PW71) in Five Families: A Rare Neutral Variant?

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

    出版 1999
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  5. 5
    MYORG is associated with recessive primary familial brain calcification

    MYORG is associated with recessive primary familial brain calcification 由 Arkadir, David, Lossos, Alexander, Rahat, Dolev, Abu Snineh, Muneer, Schueler‐Furman, Ora, Nitschke, Silvia, Minassian, Berge A., Sadaka, Yair, Lerer, Israela, Tabach, Yuval, Meiner, Vardiella

    出版 2018
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  6. 6
    A novel BRCA-1 mutation in Arab kindred from east Jerusalem with breast and ovarian cancer

    A novel BRCA-1 mutation in Arab kindred from east Jerusalem with breast and ovarian cancer 由 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

    出版 2007
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  7. 7
    KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations

    KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations 由 Klebe, Stephan, Lossos, Alexander, Azzedine, Hamid, Mundwiller, Emeline, Sheffer, Ruth, Gaussen, Marion, Marelli, Cecilia, Nawara, Magdalena, Carpentier, Wassila, Meyer, Vincent, Rastetter, Agnès, Martin, Elodie, Bouteiller, Delphine, Orlando, Laurent, Gyapay, Gabor, El-Hachimi, Khalid H, Zimmerman, Batel, Gamliel, Moriya, Misk, Adel, Lerer, Israela, Brice, Alexis, Durr, Alexandra, Stevanin, Giovanni

    出版 2012
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