Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Karim Ouldim

Showing results (21-30 of 65) with videos related to

Pageof 7
Sort By:
The Pan African Medical Journal|November 19, 2013
[Chromosome markers: case report]Imane Samri, Laila Bouguenouch, Hasna Hamdaoui, et al.
Frontiers in Genetics|October 28, 2022
Review of prostate cancer genomic studies in AfricaChaimae Samtal, Islam El Jaddaoui, Salsabil Hamdi, 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.
BMC Medical Genomics|March 19, 2026
The genetic landscape of breast cancer in young women from Morocco: implications for diagnosis and treatmentBrahim El Hejjioui, Abdelhamid Bouramtane, Laila Bouguenouch, et al.
Clinical Dysmorphology|November 6, 2025
A rare case of mosaic monosomy 21 in a Moroccan patient: clinical findings and insights from a systematic reviewAmal Ouskri, Abdelhamid Bouramtane, Rania Bouchikhi, et al.
Audiology & Neuro-Otology|January 22, 2024
Unraveling the Diversity of GJB2 Mutations in Nonsyndromic Hearing Loss: A Comprehensive Study in the Moroccan PopulationKhawla El Fizazi, Meriame Abbassi, Samira Nmer, et al.
Biomolecules|May 27, 2026
Molecular Characterization of Syndromic Hearing Loss in North African Moroccan FamiliesKhawla El Fizazi, Amama Ghaffar, Laila Bouguenouch, 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.
Lancet (London, England)|December 24, 2013
Improving medical research in the Arab worldMohammed El-Azami-El-Idrissi, Mounia Lakhdar-Idrissi, Karim Ouldim, 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.
Pageof 7

Showing results (21-30 of 65) with videos related to

Sort By:
Pageof 7
The Pan African Medical Journal|November 19, 2013
[Chromosome markers: case report]Imane Samri, Laila Bouguenouch, Hasna Hamdaoui, et al.
Frontiers in Genetics|October 28, 2022
Review of prostate cancer genomic studies in AfricaChaimae Samtal, Islam El Jaddaoui, Salsabil Hamdi, 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.
BMC Medical Genomics|March 19, 2026
The genetic landscape of breast cancer in young women from Morocco: implications for diagnosis and treatmentBrahim El Hejjioui, Abdelhamid Bouramtane, Laila Bouguenouch, et al.
Clinical Dysmorphology|November 6, 2025
A rare case of mosaic monosomy 21 in a Moroccan patient: clinical findings and insights from a systematic reviewAmal Ouskri, Abdelhamid Bouramtane, Rania Bouchikhi, et al.
Audiology & Neuro-Otology|January 22, 2024
Unraveling the Diversity of GJB2 Mutations in Nonsyndromic Hearing Loss: A Comprehensive Study in the Moroccan PopulationKhawla El Fizazi, Meriame Abbassi, Samira Nmer, et al.
Biomolecules|May 27, 2026
Molecular Characterization of Syndromic Hearing Loss in North African Moroccan FamiliesKhawla El Fizazi, Amama Ghaffar, Laila Bouguenouch, 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.
Lancet (London, England)|December 24, 2013
Improving medical research in the Arab worldMohammed El-Azami-El-Idrissi, Mounia Lakhdar-Idrissi, Karim Ouldim, 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.
Pageof 7