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Karim Ouldim

Showing results (31-40 of 65) with videos related to

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Oncology Letters|August 7, 2012
Genetic testing and first presymptomatic diagnosis in Moroccan families at high risk for breast/ovarian cancerFatima Zahra Laarabi, Imane Cherkaoui Jaouad, Karim Ouldim, et al.
BMC Research Notes|June 5, 2017
High frequency of the recurrent c.1310_1313delAAGA BRCA2 mutation in the North-East of Morocco and implication for hereditary breast-ovarian cancer prevention and controlFatima-Zahra Laarabi, Ilham Ratbi, Siham Chafai Elalaoui, et al.
Neurogenetics|January 25, 2026
Clinical and neuroimaging features in a case of cerebrotendinous xanthomatosis with a CYP27A1 genotype newly identified in morocco: a literature review of African casesAmal Ouskri, Hajar Ihlal, Oumayma Lahjouji, 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.
Genetic Testing and Molecular Biomarkers|July 26, 2018
The First Molecular Screening of MLH1 and MSH2 Genes in Moroccan Colorectal Cancer Patients Shows a Relatively High Mutational PrevalenceFatima Zahra Moufid, Laila Bouguenouch, Ihssane El Bouchikhi, et al.
Human Genome Variation|July 11, 2017
The detection of a novel insertion mutation in exon 2 of the <i>MEFV</i> gene associated with familial mediterranean fever in a moroccan familyTouhami Mejtoute, Hanane Sayel, Jamila El-Akhal, et al.
Neurogenetics|November 6, 2025
A novel homozygous loss-of-function NOTCH3 variant in a Moroccan patient: expanding the spectrum beyond CADASILAmal Ouskri, Hajar Ihlal, Zaid En-Nasery, 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.
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 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Oncology Letters|August 7, 2012
Genetic testing and first presymptomatic diagnosis in Moroccan families at high risk for breast/ovarian cancerFatima Zahra Laarabi, Imane Cherkaoui Jaouad, Karim Ouldim, et al.
BMC Research Notes|June 5, 2017
High frequency of the recurrent c.1310_1313delAAGA BRCA2 mutation in the North-East of Morocco and implication for hereditary breast-ovarian cancer prevention and controlFatima-Zahra Laarabi, Ilham Ratbi, Siham Chafai Elalaoui, et al.
Neurogenetics|January 25, 2026
Clinical and neuroimaging features in a case of cerebrotendinous xanthomatosis with a CYP27A1 genotype newly identified in morocco: a literature review of African casesAmal Ouskri, Hajar Ihlal, Oumayma Lahjouji, 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.
Genetic Testing and Molecular Biomarkers|July 26, 2018
The First Molecular Screening of MLH1 and MSH2 Genes in Moroccan Colorectal Cancer Patients Shows a Relatively High Mutational PrevalenceFatima Zahra Moufid, Laila Bouguenouch, Ihssane El Bouchikhi, et al.
Human Genome Variation|July 11, 2017
The detection of a novel insertion mutation in exon 2 of the <i>MEFV</i> gene associated with familial mediterranean fever in a moroccan familyTouhami Mejtoute, Hanane Sayel, Jamila El-Akhal, et al.
Neurogenetics|November 6, 2025
A novel homozygous loss-of-function NOTCH3 variant in a Moroccan patient: expanding the spectrum beyond CADASILAmal Ouskri, Hajar Ihlal, Zaid En-Nasery, 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.
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 7