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Imane Samri

Showing results (1-10 of 11) with videos related to

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Clinics and Research in Hepatology and Gastroenterology|January 10, 2015
TPMT alleles in the MoroccansMeryem Janati Idrissi, Imane Samri, Youssef Khabbal, et al.
The Pan African Medical Journal|February 28, 2012
[The Cri du Chat syndrome: report of an observation]Karim Ouldim, Imane Samri, Laila Bouguenouch, et al.
The Pan African Medical Journal|November 19, 2013
[Chromosome markers: case report]Imane Samri, Laila Bouguenouch, Hasna Hamdaoui, et al.
International Journal of Pediatrics & Adolescent Medicine|February 27, 2019
Noonan syndrome-causing genes: Molecular update and an assessment of the mutation rateIhssane El Bouchikhi, Khadija Belhassan, Fatima Zohra Moufid, et al.
Turkish Journal of Medical Sciences|June 19, 2015
The first PTPN1 1 mutations in hotspot exons reported in Moroccan children with Noonan syndrome and comparison of mutation rate to previous studiesIhssane El Bouchikhi, Imane Samri, Mohammed Iraqui Houssaini, et al.
The Eurasian Journal of Medicine|November 19, 2020
Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart DefectsIhssane El Bouchikhi, Laila Bouguenouch, Fatima Zohra Moufid, et al.
African Health Sciences|February 16, 2019
GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of FallotIhssane El Bouchikhi, Khadija Belhassan, Fatima Zohra Moufid, et al.
The Pan African Medical Journal|September 20, 2016
[Lynch syndrome: case report and review of the literature]Laila Bouguenouch, Imane Samri, Khadija Belhassan, et al.
Anatolian Journal of Cardiology|October 19, 2016
NKX2-5 molecular screening and assessment of variant rate and risk factors of secundum atrial septal defect in a Moroccan populationIhssane El Bouchikhi, Laila Bouguenouch, Fatima Zohra Moufid, et al.
The Pan African Medical Journal|February 28, 2012
[Microdeletion syndromes (Williams syndrome and deletion syndrome 22q11) at CHU Hassan II of Fez: report of 3 observations]Karim Ouldim, Laila Bouguenouch, Imane Samri, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Clinics and Research in Hepatology and Gastroenterology|January 10, 2015
TPMT alleles in the MoroccansMeryem Janati Idrissi, Imane Samri, Youssef Khabbal, et al.
The Pan African Medical Journal|February 28, 2012
[The Cri du Chat syndrome: report of an observation]Karim Ouldim, Imane Samri, Laila Bouguenouch, et al.
The Pan African Medical Journal|November 19, 2013
[Chromosome markers: case report]Imane Samri, Laila Bouguenouch, Hasna Hamdaoui, et al.
International Journal of Pediatrics & Adolescent Medicine|February 27, 2019
Noonan syndrome-causing genes: Molecular update and an assessment of the mutation rateIhssane El Bouchikhi, Khadija Belhassan, Fatima Zohra Moufid, et al.
Turkish Journal of Medical Sciences|June 19, 2015
The first PTPN1 1 mutations in hotspot exons reported in Moroccan children with Noonan syndrome and comparison of mutation rate to previous studiesIhssane El Bouchikhi, Imane Samri, Mohammed Iraqui Houssaini, et al.
The Eurasian Journal of Medicine|November 19, 2020
Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart DefectsIhssane El Bouchikhi, Laila Bouguenouch, Fatima Zohra Moufid, et al.
African Health Sciences|February 16, 2019
GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of FallotIhssane El Bouchikhi, Khadija Belhassan, Fatima Zohra Moufid, et al.
The Pan African Medical Journal|September 20, 2016
[Lynch syndrome: case report and review of the literature]Laila Bouguenouch, Imane Samri, Khadija Belhassan, et al.
Anatolian Journal of Cardiology|October 19, 2016
NKX2-5 molecular screening and assessment of variant rate and risk factors of secundum atrial septal defect in a Moroccan populationIhssane El Bouchikhi, Laila Bouguenouch, Fatima Zohra Moufid, et al.
The Pan African Medical Journal|February 28, 2012
[Microdeletion syndromes (Williams syndrome and deletion syndrome 22q11) at CHU Hassan II of Fez: report of 3 observations]Karim Ouldim, Laila Bouguenouch, Imane Samri, et al.
Pageof 2