Dorit Lev

6PUBLICATIONS
53CO-AUTHORS
Medical infection agents (incl. prions)Developmental genetics (incl. sex determination)Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsNeonatology
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Publications (6)

|Feb 23, 2023
Medullary Tegmental Cap Dysplasia: Fetal and Postnatal Presentations of a Unique Brainstem Malformation.

M Gafner, C Garel, Z Leibovitz

|Mar 21, 2022
Microdeletion of 16q24.1-q24.2-A unique etiology of Lymphedema-Distichiasis syndrome and neurodevelopmental disorder.

Marina Michelson, Gabriel Lidzbarsky, Daniella Nishri

|Jun 07, 2019
Refining the phenotype of the THG1L (p.Val55Ala mutation)-related mitochondrial autosomal recessive congenital cerebellar ataxia.

Melissa A Walker, Tally Lerman-Sagie, Kathryn Swoboda

|Dec 05, 2018
Prenatal and postnatal presentation of PRMT7 related syndrome: Expanding the phenotypic manifestations.

Roee Birnbaum, Naama Yosha-Orpaz, Miri Yanoov-Sharav

|Jan 23, 2015
The spinal muscular atrophy with pontocerebellar hypoplasia gene VRK1 regulates neuronal migration through an amyloid-β precursor protein-dependent mechanism.

Hadar Vinograd-Byk, Tamar Sapir, Lara Cantarero

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