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Yael Zalzstein

Rabin Medical Center

4

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Homozygous MED25 mutation implicated in eye-intellectual disability syndrome.

2015 Human Genetics
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Exome sequencing identifies mutations of both MYO7A and PDE6B in three siblings with retinitis pigmentosa

2013 Investigative Ophthalmology & Visual Science
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Genetic heterogeneity and consanguinity lead to a “double hit”: Homozygous mutations of MYO7A and PDE6B in a patient with retinitis pigmentosa

2013 Molecular Vision
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Diagnostic utility of array‐based comparative genomic hybridization (aCGH) in a prenatal setting

2010 Prenatal Diagnosis
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