Publications by authors named "Hajer Doukali"

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A novel TBX1 missense mutation in patients with syndromic congenital heart defects.
Amel Jaouadi, Mouna Tabebi, Fatma Abdelhedi, Dorra Abid, Fatma Kamoun, Hajer Doukali

Biochem Biophys Res Commun· May 2018

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Cytogenetic monitoring of hospital staff exposed to ionizing radiation: optimize protocol considering DNA repair genes variability.
Hajer Doukali, Ghada Ben Salah, Bochra Ben Rhouma, Mounira Hajjaji, Amel Jaouadi

Int J Radiat Biol· November 2017

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Oxidative stress and glutathione S-transferase genetic polymorphisms in medical staff professionally exposed to ionizing radiation.
Hajer Doukali, Ghada Ben Salah, Latifa Hamdaoui, Mounira Hajjaji, Mouna Tabebi

Int J Radiat Biol· July 2017

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Phenotypic variability in two infants sharing the same MECP2 mutation: evidence of chromosomal rearrangements and high sister-chromatid exchange levels in Rett syndrome.
Marwa Kharrat, Ines Hsairi, Hajer Doukali, Nourhene Fendri-Kriaa, Hassen Kammoun

Acta Neurol Belg· March 2017

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