Search Results - Drasinover, Valerie

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  1. 1
    Fragile-X Carrier Screening and the Prevalence of Premutation and Full-Mutation Carriers in Israel

    Fragile-X Carrier Screening and the Prevalence of Premutation and Full-Mutation Carriers in Israel by Toledano-Alhadef, Hagit, Basel-Vanagaite, Lina, Magal, Nurit, Davidov, Bella, Ehrlich, Sophie, Drasinover, Valerie, Taub, Ellen, Halpern, Gabrielle J., Ginott, Nathan, Shohat, Mordechai

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  2. 2
    Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity

    Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity by Baris, Hagit N., Barnes-Kedar, Inbal, Toledano, Helen, Halpern, Marisa, Hershkovitz, Dov, Lossos, Alexander, Lerer, Israela, Peretz, Tamar, Kariv, Revital, Cohen, Shlomi, Half, Elizabeth E., Magal, Nurit, Drasinover, Valerie, Wimmer, Katharina, Goldberg, Yael, Bercovich, Dani, Levi, Zohar

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  3. 3
    Homozygous MED25 mutation implicated in eye–intellectual disability syndrome

    Homozygous MED25 mutation implicated in eye–intellectual disability syndrome by Basel-Vanagaite, Lina, Smirin-Yosef, Pola, Essakow, Jenna Lee, Tzur, Shay, Lagovsky, Irina, Maya, Idit, Pasmanik-Chor, Metsada, Yeheskel, Adva, Konen, Osnat, Orenstein, Naama, Weisz Hubshman, Monika, Drasinover, Valerie, Magal, Nurit, Peretz Amit, Gaby, Zalzstein, Yael, Zeharia, Avraham, Shohat, Mordechai, Straussberg, Rachel, Monté, Didier, Salmon-Divon, Mali, Behar, Doron M.

    Published in Human genetics
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  4. 4
    Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis

    Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis by Basel-Vanagaite, Lina, Muncher, Liora, Straussberg, Rachel, Pasmanik-Chor, Metsada, Yahav, Michal, Rainshtein, Limor, Walsh, Christopher A., Magal, Nurit, Taub, Ellen, Drasinover, Valerie, Shalev, Hanna, Attia, Revital, Rechavi, Gideon, Simon, Amos J., Shohat, Mordechai

    Published in Annals of neurology
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  5. 5
    Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity: CMMRD, Founder Mutations, and Consanguinity in Israel

    Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity: CMMRD, Founder Mutations, and Consanguinity in Israel by Baris, Hagit N., Barnes-Kedar, Inbal, Toledano, Helen, Halpern, Marisa, Hershkovitz, Dov, Lossos, Alexander, Lerer, Israela, Peretz, Tamar, Kariv, Revital, Cohen, Shlomi, Half, Elizabeth E., Magal, Nurit, Drasinover, Valerie, Wimmer, Katharina, Goldberg, Yael, Bercovich, Dani, Levi, Zohar

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  6. 6
    Amniotic trisomy 11 mosaicism-is it a benign finding?

    Amniotic trisomy 11 mosaicism-is it a benign finding? by Basel-Vanagaite, Lina, Davidov, Bella, Friedman, Jane, Yeshaya, Yosefa, Magal, Nurit, Drasinover, Valerie, Shohat, Mordechai

    Published in Prenatal diagnosis
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  7. 7
    Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotes

    Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotes by Drasinover, Valerie, Ehrlich, Sophia, Magal, Nurit, Taub, Ellen, Libman, Vitalia, Shohat, Tamy, Halpern, Gabrielle J., Shohat, Mordechai

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  8. 8
    Increased transmission of intermediate alleles of theFMR1 gene compared with normal alleles among female heterozygotes

    Increased transmission of intermediate alleles of theFMR1 gene compared with normal alleles among female heterozygotes by Drasinover, Valerie, Ehrlich, Sophia, Magal, Nurit, Taub, Ellen, Libman, Vitalia, Shohat, Tamy, Halpern, Gabrielle J., Shohat, Mordechai

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