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Afaf Ben Itto
Observed names:
A. Ben Itto,
Afaf Ben Iitto,
AfafBen Itto,
Ben Itto, Afaf
Observed institution:
Centre Hospitalier Universitaire Ibn Rochd
OpenAlex ID:
A5076940587
Evolution of Molecular Diagnosis of Duchenne Muscular Dystrophy
2013
·
Afaf Ben Itto
, Khalil Hamzi
, et al.
·
Journal of Molecular Neuroscience
·
10
Prenatal Diagnosis of BMD in Morocco: Evolution and Limits
2013
·
Khalil Hamzi
, Afaf Ben Itto
, et al.
·
Journal of Molecular Neuroscience
·
6
Prader-Willi syndrome: Methylation study or fluorescence in situ hybridization first?
2010
·
Sellama Nadifi
, Khalil Hamzi
, et al.
·
Indian journal of human genetics
·
5
A Case Report: Identification of a Pathogenic Microdeletion at Chromosome 21q21.3q22.13 Using Whole-Exome Sequencing and CNV Analysis in a Moroccan Child with Global Developmental Delay
2025
·
Farah Jouali
, Ghyzlane El Haddoumi
, et al.
·
Genes
·
1
PDF
Angelman Syndrome: Etiologies and Genetic Counseling
2014
·
Khalil Hamzi
, Afaf Ben Itto
, et al.
Syndrome de Bart : une nouvelle observation néonatale
2013
·
A. Ben Itto
, M. Lehlimi
, et al.
·
Journal de Pédiatrie et de Puériculture
Sickle Cell Disease with Double Stroke in a Moroccan Family
2013
·
Khalil Hamzi
, Afaf Ben Itto
, et al.
·
Journal of Molecular Neuroscience
Profil étiologique des DIP au Maroc ( A propos de 230 cas)
2010
·
Ben Itto, Afaf
·
Toubkal
Profil étiologique des DIP au Maroc (A propos de 230 cas)
2010
·
Afaf Ben Iitto
·
Toubkal
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Works count:
11
Citation count:
22
H-index:
3
I10-index:
1
Year
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