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Laila Bouguenouch

Showing results (1-10 of 71) 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
Cureus|September 22, 2025
A De Novo 13q21.33-q31.1 Interstitial Deletion in a Child With Megalocornea and Neurodevelopmental Delay: A Clinico-Genomic CorrelationBadreddine Elmakhzen, Ayoub Nedbour, Laila Bouguenouch, et al.
Cureus|May 4, 2023
A Mosaic PIK3CA Mutation in a Moroccan Female: Exploring the Diagnostic Challenges of PIK3CA-Related Overgrowth SpectrumMohamed Ahakoud, Hanae Daha Belghiti, Hajar Ihlal, et al.
Frontiers in Genetics|January 25, 2024
The burden of cystic fibrosis in North AfricaNada El Makhzen, Houria Daimi, Laila Bouguenouch, et al.
The Pan African Medical Journal|November 7, 2019
[Kallmann-de Morsier syndrome: about 3 cases]Halima Marhari, Fatima Zahra Chahdi Ouazzani, Hanan El Ouahabi, et al.
La Tunisie Medicale|March 17, 2025
Investigation of 22q11.2 Deletion Syndrome in the first Moroccan Pediatric Patients seriesAsmaa Gaadi, Ahmed Aziz Bousfiha, Said Trhanint, 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.
Molecular Biology Reports|December 1, 2024
Atypical presentation of Dyggve-Melchior-Clausen disease in a Moroccan child without developmental delay and intellectual disabilitiesBadreddine Elmakhzen, Laila Bouguenouch, Kettani Oussama, 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.
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 8

Showing results (1-10 of 71) with videos related to

Sort By:
Pageof 8
Cancer Genetics|June 12, 2026
Molecular etiology and therapeutic advances in retinoblastomaMaryem Ouarhache, Laila Bouguenouch, Karim Ouldim
Cureus|September 22, 2025
A De Novo 13q21.33-q31.1 Interstitial Deletion in a Child With Megalocornea and Neurodevelopmental Delay: A Clinico-Genomic CorrelationBadreddine Elmakhzen, Ayoub Nedbour, Laila Bouguenouch, et al.
Cureus|May 4, 2023
A Mosaic PIK3CA Mutation in a Moroccan Female: Exploring the Diagnostic Challenges of PIK3CA-Related Overgrowth SpectrumMohamed Ahakoud, Hanae Daha Belghiti, Hajar Ihlal, et al.
Frontiers in Genetics|January 25, 2024
The burden of cystic fibrosis in North AfricaNada El Makhzen, Houria Daimi, Laila Bouguenouch, et al.
The Pan African Medical Journal|November 7, 2019
[Kallmann-de Morsier syndrome: about 3 cases]Halima Marhari, Fatima Zahra Chahdi Ouazzani, Hanan El Ouahabi, et al.
La Tunisie Medicale|March 17, 2025
Investigation of 22q11.2 Deletion Syndrome in the first Moroccan Pediatric Patients seriesAsmaa Gaadi, Ahmed Aziz Bousfiha, Said Trhanint, 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.
Molecular Biology Reports|December 1, 2024
Atypical presentation of Dyggve-Melchior-Clausen disease in a Moroccan child without developmental delay and intellectual disabilitiesBadreddine Elmakhzen, Laila Bouguenouch, Kettani Oussama, 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.
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.
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