Publications by authors named "Dina Fine"

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A multicenter study reveals a novel pathogenic splice-site founder variant in OTOF.
Zippora Brownstein, Lara Kamal, Shir Mishan-Montefiori, Yael Hoffman, Dina Fine

Hum Genomics· October 2025

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A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4A.
Dina Fine, Hagit Flusser, Barak Markus, Zamir Shorer, Libe Gradstein

Eur J Hum Genet· December 2015

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Mutations disrupting selenocysteine formation cause progressive cerebello-cerebral atrophy.
Orly Agamy, Bruria Ben Zeev, Dorit Lev, Barak Marcus, Dina Fine

Am J Hum Genet· October 2010

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