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Yahya BENBOUCHTA

Observed names: BENBOUCHTA Yahya, BENBOUCHTA, Y., Benbouchta Yahya, Yahya Benbouchta
ORCID: 0000-0001-6276-1065
Observed ORCID: 0000-0001-6276-1065
OpenAlex ID: A5014865722
15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review
2021 · Yahya Benbouchta, Nicole De Leeuw, et al. · The Italian Journal of Pediatrics/Italian journal of pediatrics · 18
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Cytogenetic Analysis of 5572 Patients Referred for Suspected Chromosomal Abnormalities in Morocco
2012 · Nisrine Aboussair, Imane Cherkaoui Jaouad, et al. · Genetic Testing and Molecular Biomarkers · 17
Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report
2021 · Yahya Benbouchta, Imane Cherkaoui Jaouad, et al. · BMC Medical Genomics · 3
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Research of the Philadelphia Chromosome in Chronic Myeloid Leukemia: Diagnostic and Prognostic Interests
2021 · Yahya Benbouchta, Ahmed Afailal Tribak, et al. · IntechOpen eBooks · 1
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Caractérisation génomique de deux maladies génétiques rares : la cardiopathie congénitale syndromique et la dystrophie cornéenne atypique & Intérêt des gènes identifiés dans ces deux maladies dans la prédisposition génétique au cancer
2021 · BENBOUCHTA Yahya · Toubkal
Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report
2020 · Yahya BENBOUCHTA, Imane CHERKAOUI JAOUAD, et al.
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Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report
2020 · Yahya BENBOUCHTA, Imane CHERKAOUI JAOUAD, et al.
PDF
Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report.
2020 · Yahya BENBOUCHTA, Imane CHERKAOUI JAOUAD, et al.
PDF
Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy
2020 · Yahya BENBOUCHTA, Imane CHERKAOUI JAOUAD, et al.
PDF
Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy
2020 · Yahya BENBOUCHTA, Imane CHERKAOUI, et al.
PDF
Intérêt Du Chromosome Philadelphie Dans Les Syndromes Myéloprolifératifs
2013 · BELKHAYYAT HASSANI, A., BENBOUCHTA, Y., et al. · Maroc médical
Works count: 11
Citation count: 39
H-index: 3
I10-index: 2
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