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Mouna Ben Amor

Showing results (1-10 of 23) with videos related to

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Heliyon|October 16, 2023
Dividend policy and crisis: Exploring the interplay between performance and financial constraints in the French contextSaliha Theiri, Salah Ben Hamad, Mouna Ben Amor
Case Reports in Medicine|June 11, 2025
The Reclassification of a <i>FBN1</i> Variant of Unknown Significance Associated With Marfan Syndrome Through Careful Clinical Correlation and Family-Based EvaluationDominique Bouhamdani, Véronique Allain, Nadia Bouhamdani, et al.
Journal of Osteoporosis|September 14, 2011
Genotype-phenotype correlations in autosomal dominant osteogenesis imperfectaI Mouna Ben Amor, Francis H Glorieux, Frank Rauch
Pediatric Endocrinology Reviews : PER|July 18, 2013
Osteogenesis imperfectaMouna Ben Amor, Frank Rauch, Elena Monti, et al.
European Journal of Medical Genetics|October 15, 2014
Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly in a Finnish woman: first confirmation of a duplication in RUNX2 as pathogenic variantKristiina Avela, Heljä Hirvinen, Mouna Ben Amor, et al.
European Journal of Medical Genetics|June 12, 2023
Novel dermatological and skeletal features associated with PTEN variant in PTEN hamartoma tumor syndromeDominique Comeau, Véronique Allain, Nicole Maillet-Lebel, et al.
The Journal of Clinical Endocrinology and Metabolism|May 29, 2012
Abnormalities in muscle density and muscle function in hypophosphatemic ricketsLouis-Nicolas Veilleux, Moira Cheung, Mouna Ben Amor, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 27, 2013
Skeletal clinical characteristics of osteogenesis imperfecta caused by haploinsufficiency mutations in COL1A1I Mouna Ben Amor, Peter Roughley, Francis H Glorieux, et al.
Frontiers in Genetics|March 1, 2024
Diagnostic utility of DNA methylation episignature analysis for early diagnosis of KMT2B-related disorders: case reportNadia Bouhamdani, Haley McConkey, Amélie Leblanc, et al.
European Journal of Medical Genetics|October 8, 2025
Corrigendum to "A novel RORA genetic variant associated with early-onset obesity and insomnia"Alexie Ouellette, Eric P Allain, Abdullah Almaghraby, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Heliyon|October 16, 2023
Dividend policy and crisis: Exploring the interplay between performance and financial constraints in the French contextSaliha Theiri, Salah Ben Hamad, Mouna Ben Amor
Case Reports in Medicine|June 11, 2025
The Reclassification of a <i>FBN1</i> Variant of Unknown Significance Associated With Marfan Syndrome Through Careful Clinical Correlation and Family-Based EvaluationDominique Bouhamdani, Véronique Allain, Nadia Bouhamdani, et al.
Journal of Osteoporosis|September 14, 2011
Genotype-phenotype correlations in autosomal dominant osteogenesis imperfectaI Mouna Ben Amor, Francis H Glorieux, Frank Rauch
Pediatric Endocrinology Reviews : PER|July 18, 2013
Osteogenesis imperfectaMouna Ben Amor, Frank Rauch, Elena Monti, et al.
European Journal of Medical Genetics|October 15, 2014
Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly in a Finnish woman: first confirmation of a duplication in RUNX2 as pathogenic variantKristiina Avela, Heljä Hirvinen, Mouna Ben Amor, et al.
European Journal of Medical Genetics|June 12, 2023
Novel dermatological and skeletal features associated with PTEN variant in PTEN hamartoma tumor syndromeDominique Comeau, Véronique Allain, Nicole Maillet-Lebel, et al.
The Journal of Clinical Endocrinology and Metabolism|May 29, 2012
Abnormalities in muscle density and muscle function in hypophosphatemic ricketsLouis-Nicolas Veilleux, Moira Cheung, Mouna Ben Amor, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 27, 2013
Skeletal clinical characteristics of osteogenesis imperfecta caused by haploinsufficiency mutations in COL1A1I Mouna Ben Amor, Peter Roughley, Francis H Glorieux, et al.
Frontiers in Genetics|March 1, 2024
Diagnostic utility of DNA methylation episignature analysis for early diagnosis of KMT2B-related disorders: case reportNadia Bouhamdani, Haley McConkey, Amélie Leblanc, et al.
European Journal of Medical Genetics|October 8, 2025
Corrigendum to "A novel RORA genetic variant associated with early-onset obesity and insomnia"Alexie Ouellette, Eric P Allain, Abdullah Almaghraby, et al.
Pageof 3