Michal Feingold-Zadok

Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22

Rony Cohen, Lina Basel‐Vanagaite, Hadassah Goldberg‐Stern et al. · European Journal of Paediatric Neurology · 2014 · 31 citations

Life Sciences, Genetics, Molecular Genetics +12

Mutations in the <i>NEB</i> gene cause fetal akinesia/arthrogryposis multiplex congenita

Michal Feingold-Zadok, David Chitayat, Karen Chong et al. · Prenatal Diagnosis · 2016 · 28 citations

Life Sciences, Genetics, Molecular Genetics +13

Expanding the Mutational Spectrum of<i>CRLF1</i>in Crisponi/CISS1 Syndrome

Roberta Piras, Francesca Chiappe, Ilaria La Torraca et al. · Human Mutation · 2014 · 26 citations

Life Sciences, Genetics, Molecular Genetics +11

Terminal microdeletions of 13q34 chromosome region in patients with intellectual disability: Delineation of an emerging new microdeletion syndrome

Eyal Reinstein, Meytal Liberman, Michal Feingold-Zadok et al. · Molecular Genetics and Metabolism · 2016 · 23 citations

Life Sciences, Genetics, Molecular Genetics +17

Risk of Clinically Significant Chromosomal Microarray Analysis Findings in Fetuses With Nuchal Translucency From 3.0 mm Through 3.4 mm

Lena Sagi‐Dain, Amihood Singer, Shay Ben Shachar et al. · Obstetrics and Gynecology · 2020 · 20 citations

Medicine, Genetics, Obstetrics +17