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Search Results - Doukali, Hajer
Search Results - Doukali, Hajer
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A novel TBX1 missense mutation in patients with syndromic congenital heart defects
by
Jaouadi, Amel
,
Tabebi, Mouna
,
Abdelhedi, Fatma
,
Abid, Dorra
,
Kamoun, Fatma
,
Chabchoub, Imen
,
Maatoug, Sirine
,
Doukali, Hajer
,
Belghuith, Neila
,
Ksentini, Mohamed Ali
,
Keskes, Leila Ammar
,
Triki, Chahnez
,
Hachicha, Mongia
,
Kamoun, Samir
,
Kamoun, Hassen
Published in
Biochemical and biophysical research communications
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Oxidative stress and glutathione S-transferase genetic polymorphisms in medical staff professionally exposed to ionizing radiation
by
Doukali, Hajer
,
Ben Salah, Ghada
,
Hamdaoui, Latifa
,
Hajjaji, Mounira
,
Tabebi, Mouna
,
Ammar-Keskes, Leila
,
Masmoudi, Mohamed-Elarbi
,
Kamoun, Hassen
Published in
International journal of radiation biology
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Cytogenetic monitoring of hospital staff exposed to ionizing radiation: optimize protocol considering DNA repair genes variability
by
Doukali, Hajer
,
Ben Salah, Ghada
,
Ben Rhouma, Bochra
,
Hajjaji, Mounira
,
Jaouadi, Amel
,
Belguith-Mahfouth, Neila
,
Masmoudi, Mohamed-Larbi
,
Ammar-Keskes, Leila
,
Kamoun, Hassen
Published in
International journal of radiation biology
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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
by
Kharrat, Marwa
,
Hsairi, Ines
,
Doukali, Hajer
,
Fendri-Kriaa, Nourhene
,
Kammoun, Hassen
,
Ammar-keskes, Leila
,
Triki, Chahnez
,
Fakhfakh, Faiza
Published in
Acta neurologica Belgica
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Occupational Exposure - Analysis
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Tunisia
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22Q11.2Deletion Syndrome
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