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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)

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|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

|Oct 28, 2020

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1.

Zippora Brownstein, Suleyman Gulsuner, Tom Walsh

|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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Frequent Collaborators

2 joint publications

Michal Gafner

1 joint publications

C Garel

1 joint publications

S Valence

1 joint publications

K Krajden Haratz

1 joint publications

R Oegema

1 joint publications

G M S Mancini

1 joint publications

D Heron

1 joint publications

E Bueltmann

1 joint publications

L Burglen

1 joint publications

D Rodriguez

Frequent Collaborators

2 joint publications

Michal Gafner

1 joint publications

C Garel

1 joint publications

S Valence

1 joint publications

K Krajden Haratz

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