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Edna Ben-Asher

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American Journal of Human Genetics|November 27, 2012

Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesisDanit Oz-Levi, Bruria Ben-Zeev, Elizabeth K Ruzzo, et al.

FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 8, 2010

Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidenceFederica Torri, Anna Akelai, Sara Lupoli, et al.

American Journal of Human Genetics|November 16, 2002

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1Orly Dgany, Nili Avidan, Jean Delaunay, et al.

Neuron|October 22, 2013

Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathyElizabeth K Ruzzo, José-Mario Capo-Chichi, Bruria Ben-Zeev, et al.

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Search research articles

Showing results (21-30 of 24) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 24 results.

American Journal of Human Genetics|November 27, 2012

Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesisDanit Oz-Levi, Bruria Ben-Zeev, Elizabeth K Ruzzo, et al.

FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 8, 2010

Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidenceFederica Torri, Anna Akelai, Sara Lupoli, et al.

American Journal of Human Genetics|November 16, 2002

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1Orly Dgany, Nili Avidan, Jean Delaunay, et al.

Neuron|October 22, 2013

Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathyElizabeth K Ruzzo, José-Mario Capo-Chichi, Bruria Ben-Zeev, et al.

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