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Homozygous MED25 mutation implicated in eye-intellectual disability syndrome.
Hum Genet. 2015 Jun;134(6):577-87. doi: 10.1007/s00439-015-1541-x. Epub 2015 Mar 20.
Hum Genet. 2015.
PMID: 25792360
Clinical Trial.
Genetic heterogeneity and consanguinity lead to a "double hit": homozygous mutations of MYO7A and PDE6B in a patient with retinitis pigmentosa.
Goldenberg-Cohen N, Banin E, Zalzstein Y, Cohen B, Rotenstreich Y, Rizel L, Basel-Vanagaite L, Ben-Yosef T.
Goldenberg-Cohen N, et al. Among authors: zalzstein y.
Mol Vis. 2013 Jul 20;19:1565-71. Print 2013.
Mol Vis. 2013.
PMID: 23882135
Free PMC article.
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Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting.
Maya I, Davidov B, Gershovitz L, Zalzstein Y, Taub E, Coppinger J, Shaffer LG, Shohat M.
Maya I, et al. Among authors: zalzstein y.
Prenat Diagn. 2010 Dec;30(12-13):1131-7. doi: 10.1002/pd.2626.
Prenat Diagn. 2010.
PMID: 20925131
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A dual role for interleukin-1 in hippocampal-dependent memory processes.
Goshen I, Kreisel T, Ounallah-Saad H, Renbaum P, Zalzstein Y, Ben-Hur T, Levy-Lahad E, Yirmiya R.
Goshen I, et al. Among authors: zalzstein y.
Psychoneuroendocrinology. 2007 Sep-Nov;32(8-10):1106-15. doi: 10.1016/j.psyneuen.2007.09.004. Epub 2007 Oct 31.
Psychoneuroendocrinology. 2007.
PMID: 17976923
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