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Karim Ouldim

Showing results (1-10 of 65) with videos related to

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Cancer Genetics|June 12, 2026
Molecular etiology and therapeutic advances in retinoblastomaMaryem Ouarhache, Laila Bouguenouch, Karim Ouldim
Molecular Genetics & Genomic Medicine|November 30, 2016
Genetics and genomic medicine in Morocco: the present hope can make the future brightKhadija Belhassan, Karim Ouldim, Abdel Aziz Sefiani
Journal of Biomedicine & Biotechnology|June 2, 2007
Tetrasomy 15q11-q13 diagnosed by FISH in a patient with autistic disorderKarim Ouldim, Abdelhafid Natiq, Philippe Jonveaux, et al.
Joint Bone Spine|December 16, 2011
Multiple synostosis syndromeHicham Hachimi, Latifa Tahiri, Najoua Ghani, et al.
Molecular Biology Reports|May 25, 2024
A novel homozygous missense variant identified in the myosin VIIA motor domain of a Moroccan patient with usher syndromeMaryem Ouarhache, Oussama Kettani, Khawla El Fizazi, et al.
Annales De Biologie Clinique|August 15, 2014
[Pharmacogenetics and prediction of side effects of drugs]Mohammed Harrak, Youssef Khabbal, Afaf Amarti, et al.
Clinics and Research in Hepatology and Gastroenterology|January 10, 2015
TPMT alleles in the MoroccansMeryem Janati Idrissi, Imane Samri, Youssef Khabbal, et al.
Molecular Genetics and Metabolism Reports|March 3, 2026
First combined analysis of <i>SMN1</i>, <i>SMN2</i>, and <i>NAIP</i> copy numbers in Moroccan SMA patients and their correlation with disease severitySamira Nmer, Said Trhanint, Hanane Sayel, et al.
The Pan African Medical Journal|June 21, 2013
[Pharmacogenetics: what about Morocco?]Meryem Janati Idrissi, Karim Ouldim, Afaf Amarti, et al.
Cureus|July 4, 2024
Exploring Splice-Site Mutations in LAMA2-Related Muscular Dystrophies: A Comprehensive Analysis of Genotypic and Phenotypic PatternsSamira Nmer, Amina Ameli, Said Trhanint, et al.
Pageof 7

Showing results (1-10 of 65) with videos related to

Sort By:
Pageof 7
Cancer Genetics|June 12, 2026
Molecular etiology and therapeutic advances in retinoblastomaMaryem Ouarhache, Laila Bouguenouch, Karim Ouldim
Molecular Genetics & Genomic Medicine|November 30, 2016
Genetics and genomic medicine in Morocco: the present hope can make the future brightKhadija Belhassan, Karim Ouldim, Abdel Aziz Sefiani
Journal of Biomedicine & Biotechnology|June 2, 2007
Tetrasomy 15q11-q13 diagnosed by FISH in a patient with autistic disorderKarim Ouldim, Abdelhafid Natiq, Philippe Jonveaux, et al.
Joint Bone Spine|December 16, 2011
Multiple synostosis syndromeHicham Hachimi, Latifa Tahiri, Najoua Ghani, et al.
Molecular Biology Reports|May 25, 2024
A novel homozygous missense variant identified in the myosin VIIA motor domain of a Moroccan patient with usher syndromeMaryem Ouarhache, Oussama Kettani, Khawla El Fizazi, et al.
Annales De Biologie Clinique|August 15, 2014
[Pharmacogenetics and prediction of side effects of drugs]Mohammed Harrak, Youssef Khabbal, Afaf Amarti, et al.
Clinics and Research in Hepatology and Gastroenterology|January 10, 2015
TPMT alleles in the MoroccansMeryem Janati Idrissi, Imane Samri, Youssef Khabbal, et al.
Molecular Genetics and Metabolism Reports|March 3, 2026
First combined analysis of <i>SMN1</i>, <i>SMN2</i>, and <i>NAIP</i> copy numbers in Moroccan SMA patients and their correlation with disease severitySamira Nmer, Said Trhanint, Hanane Sayel, et al.
The Pan African Medical Journal|June 21, 2013
[Pharmacogenetics: what about Morocco?]Meryem Janati Idrissi, Karim Ouldim, Afaf Amarti, et al.
Cureus|July 4, 2024
Exploring Splice-Site Mutations in LAMA2-Related Muscular Dystrophies: A Comprehensive Analysis of Genotypic and Phenotypic PatternsSamira Nmer, Amina Ameli, Said Trhanint, et al.
Pageof 7