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NARA Subscribed3
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Springer Nature3
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Human Genetics2
NeuroMolecular Medicine1
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20152
20131
Yakov Fellig results 3 · Newest (Page 1/1, per page 25)
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Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5NARA Subscribed
Human Genetics · 2015 · Vol. 134 · Issue 3 · Springer
Daniella Magen; Ayala Ofir; Liron Berger; Dorit Goldsher; Ayelet Eran; Nasser Katib; Yousif Nijem; Euvgeni Vlodavsky; Shay Tzur; Doron M. Behar; Yakov Fellig; Hanna Mandel
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Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5NARA Subscribed
Human Genetics · 2015 · Vol. 134 · Issue 3 · Springer
Daniella Magen; Ayala Ofir; Liron Berger; Dorit Goldsher; Ayelet Eran; Nassser Katib; Yousif Nijem; Euvgeni Vlodavsky; Shay Zur; Doron M. Behar; Yakov Fellig; Hanna Mandel
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Variable Phenotypes of Knockin Mice Carrying the M712T Gne MutationNARA Subscribed
NeuroMolecular Medicine · 2013 · Vol. 15 · Issue 1 · Springer
Ilan Sela; Lena Yakovlev; Michal Becker Cohen; Moran Elbaz; Nurit Yanay; Uri Ben Shlomo; Hagit Yotvat; Yakov Fellig; Zohar Argov; Stella Mitrani-Rosenbaum
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