Publications by authors named "Imane Samri"

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Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects.
Ihssane El Bouchikhi, Laila Bouguenouch, Fatima Zohra Moufid, Khadija Belhassan, Imane Samri

Eurasian J Med· October 2020

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GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot.
Ihssane El Bouchikhi, Khadija Belhassan, Fatima Zohra Moufid, Mohammed Iraqui Houssaini, Laila Bouguenouch, Imane Samri

Afr Health Sci· December 2018

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[Fanconi anemia at the University Hospital (CHU) Hassan II of Fez: about 6 cases].
Laila Bouguenouch, Imane Samri, Meryem Abbassi, Hasna Hamdaoui, Ihssane El Otmani

Pan Afr Med J· July 2018

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NKX2-5 molecular screening and assessment of variant rate and risk factors of secundum atrial septal defect in a Moroccan population.
Ihssane El Bouchikhi, Laila Bouguenouch, Fatima Zohra Moufid, Mohammed Iraqui Houssaini, Khadija Belhassan, Imane Samri

Anatol J Cardiol· March 2017

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[Lynch syndrome: case report and review of the literature].
Laila Bouguenouch, Imane Samri, Khadija Belhassan, Hanane Sayel, Meriame Abbassi

Pan Afr Med J· February 2017

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Noonan syndrome-causing genes: Molecular update and an assessment of the mutation rate.
Ihssane El Bouchikhi, Khadija Belhassan, Fatima Zohra Moufid, Mohammed Iraqui Houssaini, Laila Bouguenouch, Imane Samri

Int J Pediatr Adolesc Med· December 2016

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TPMT alleles in the Moroccans.
Meryem Janati Idrissi, Imane Samri, Youssef Khabbal, Mohammed El Hassouni, Karim Ouldim

Clin Res Hepatol Gastroenterol· September 2015

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The first PTPN1 1 mutations in hotspot exons reported in Moroccan children with Noonan syndrome and comparison of mutation rate to previous studies.
Ihssane El Bouchikhi, Imane Samri, Mohammed Iraqui Houssaini, Saaid Trhanint, Laila Bouguenouch

Turk J Med Sci· July 2015

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[Chromosome markers: case report].
Imane Samri, Laila Bouguenouch, Hasna Hamdaoui, Ihsan El Otmani, Nissrine El Omairi

Pan Afr Med J· December 2014

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[Microdeletion syndromes (Williams syndrome and deletion syndrome 22q11) at CHU Hassan II of Fez: report of 3 observations].
Karim Ouldim, Laila Bouguenouch, Imane Samri, Ihsan El Otmani, Hasna Hamdaoui

Pan Afr Med J· June 2012

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[The Cri du Chat syndrome: report of an observation].
Karim Ouldim, Imane Samri, Laila Bouguenouch, Hasna Hamdaoui, Ihsan El Otmani

Pan Afr Med J· June 2012

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