Search Results - Lerer, Israela

  • Showing 1 - 7 results of 7
Refine Results
  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 by Silverstein, Shira, Lerer, Israela, Buiting, Karin, Abeliovich, Dvorah

    Published 2001
    Get full text Get full text
    Text
    Save to List
    Saved in:
  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 by Molho-Pessach, Vered, Lerer, Israela, Abeliovich, Dvorah, Agha, Ziad, Abu Libdeh, Abdulasalam, Broshtilova, Valentina, Elpeleg, Orly, Zlotogorski, Abraham

    Published 2008
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  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 by Wimplinger, Isabella, Morleo, Manuela, Rosenberger, Georg, Iaconis, Daniela, Orth, Ulrike, Meinecke, Peter, Lerer, Israela, Ballabio, Andrea, Gal, Andreas, Franco, Brunella, Kutsche, Kerstin

    Published 2006
    Get full text Get full text
    Text
    Save to List
    Saved in:
  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? by Buiting, Karin, Dittrich, Bärbel, Dworniczak, Bernd, Lerer, Israela, Abeliovich, Dvorah, Cottrell, Sally, Temple, I. Karen, Harvey, John F., Lich, Christina, Groß, Stephanie, Horsthemke, Bernhard

    Published 1999
    Get full text Get full text
    Text
    Save to List
    Saved in:
  5. 5
    MYORG is associated with recessive primary familial brain calcification

    MYORG is associated with recessive primary familial brain calcification by 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

    Published 2018
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  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 by 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

    Published 2007
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:
  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 by 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

    Published 2012
    Get full text Get full text Get full text
    Text
    Save to List
    Saved in:

Search Tools: