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List of works by Elon Pras

Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects.

scientific article published on 18 July 2016

Prenatal diagnosis for de novo mutations: Experience from a tertiary center over a 10-year period

scientific article published on 28 January 2019

SMYD1 is the underlying gene for the AnWj-negative blood group phenotype

scientific article published on 03 August 2018

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

scientific article published on 24 August 2020

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