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Novel EXOSC3 mutation causes complicated hereditary spastic paraplegia. [electronic resource] by
- Halevy, Ayelet
- Lerer, Israela
- Cohen, Rony
- Kornreich, Liora
- Shuper, Avinoam
- Gamliel, Moria
- Zimerman, Bat-El
- Korabi, Isam
- Meiner, Vardiella
- Straussberg, Rachel
- Lossos, Alexander
Producer: 20150724
In:
Journal of neurology vol. 261
Availability: No items available.
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17.
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Kyphoscoliosis peptidase (KY) mutation causes a novel congenital myopathy with core targetoid defects. [electronic resource] by
- Straussberg, Rachel
- Schottmann, Gudrun
- Sadeh, Menachem
- Gill, Esther
- Seifert, Franziska
- Halevy, Ayelet
- Qassem, Kaiyal
- Rendu, John
- van der Ven, Peter F M
- Stenzel, Werner
- Schuelke, Markus
Producer: 20180116
In:
Acta neuropathologica vol. 132
Availability: No items available.
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18.
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Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene. [electronic resource] by
- Blumkin, Lubov
- Halevy, Ayelet
- Ben-Ami-Raichman, Dominique
- Dahari, Dvir
- Haviv, Ami
- Sarit, Cohen
- Lev, Dorit
- van der Knaap, Marjo S
- Lerman-Sagie, Tally
- Leshinsky-Silver, Esther
Producer: 20150528
In:
Neurogenetics vol. 15
Availability: No items available.
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19.
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Reply to: The many faces of TUBB4A mutations. [electronic resource] by
- Blumkin, Lubov
- Halevy, Ayelet
- Ben-Ami-Raichman, Dominique
- Dahari, Dvir
- Haviv, Ami
- Sarit, Cohen
- Lev, Dorit
- van der Knaap, Marjo S
- Lerman-Sagie, Tally
- Leshinsky-Silver, Esther
Producer: 20150528
In:
Neurogenetics vol. 15
Availability: No items available.
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20.
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Microcephaly-thin corpus callosum syndrome maps to 8q23.2-q24.12. [electronic resource] by
- Halevy, Ayelet
- Basel-Vanagaite, Lina
- Shuper, Avinoam
- Helman, Shlomit
- Har-Zahav, Adi
- Birk, Efrat
- Maya, Idit
- Kornreich, Liora
- Inbar, Dov
- Nürnberg, Gudrun
- Nürnberg, Peter
- Steinberg, Tamar
- Straussberg, Rachel
Producer: 20130329
In:
Pediatric neurology vol. 46
Availability: No items available.
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