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Aziza Sbiti

Observed names: A Sbiti, A. SBITI, A. Sbiti, SBITI, A., Sbiti, Aziza
OpenAlex ID: A5079645490
Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis
2007 · Lekbir Baala, Sylvain Briault, et al. · Nature Genetics · 212
Consanguineous Marriages in Morocco and the Consequence for the Incidence of Autosomal Recessive Disorders
2009 · I. CHERKAOUI JAOUAD, S. CHAFAÏ ELALAOUI, et al. · Journal of Biosocial Science · 131
Unexpected fertility and paternal UPD 22
2008 · Karim Ouldim, Aziza Sbiti, et al. · Fertility and Sterility · 75
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Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients
2002 · Aziza Sbiti, Fatiha El Kerch, et al. · BioMed Research International · 32
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Spinal Muscular Atrophy Carrier Frequency and Estimated Prevalence of the Disease in Moroccan Newborns
2011 · Jaber Lyahyai, Aziza Sbiti, et al. · Genetic Testing and Molecular Biomarkers · 28
Carrier Frequency of the c.525delT Mutation in the SGCG Gene and Estimated Prevalence of Limb Girdle Muscular Dystrophy Type 2C Among the Moroccan Population
2014 · Fatiha El Kerch, Ilham Ratbi, et al. · Genetic Testing and Molecular Biomarkers · 26
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
Cytogenetic and epidemiological profiles of Down syndrome in a Moroccan population: a report of 852 cases.
2010 · I C Jaouad, S Cherkaoui Deqaqi, et al. · PubMed · 17
A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11.
1998 · S C Deqaqi, M N'Guessan, et al. · PubMed · 10
Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report
2016 · Saadia Amasdl, Abdelhafid Natiq, et al. · Journal of Medical Case Reports · 8
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20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature
2016 · Saadia Amasdl, Abdelhafid Natiq, et al. · BMC Research Notes · 8
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Molecular diagnosis of dystrophinopathies in Morocco and report of six novel mutations
2020 · Youssef EL Kadiri, Yassir Selouani, et al. · Clinica Chimica Acta · 6
Cytogenetic Investigation in a Group of Ten Infertile Men with Non-Obstructive Azoospermia: First Algerian 46, XX Syndrome.
2016 · Meriem Baziz, Zohra Hamouli-Said, et al. · PubMed Central · 5
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Familial X/Y Translocation Encompassing ARSE in Two Moroccan Siblings with Sensorineural Deafness
2017 · Saadia Amasdl, Wiam Smaili, et al. · Cytogenetic and Genome Research · 4
L’amyotrophie spinale infantile : cause fréquente des hypotonies congénitales au Maroc
2011 · A. Sbiti, I. Ratbi, et al. · Archives de Pédiatrie · 3
Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report
2023 · Zhour El Amrani, Abdelhafid Natiq, et al. · Molecular Syndromology · 2
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Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemia
2021 · Yassamine Doubaj, Abdelali Zrhidri, et al. · Pan African Medical Journal · 2
Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability
2022 · Zhour EL Amrani, Siham Chafai Elalaoui, et al. · Ophthalmic Genetics · 1
Constitutional Partial Proximal Trisomy 14q11.2 to 14q21: Two New Moroccan Cases and Review of the Literature
2019 · Hanane Merhmi, Maria Zerkaoui, et al. · OBM Genetics · 1
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Genetic and allelic heterogeneity of LGMD in North Africa
1997 · K. Azibi, M. Chaouch, et al. · Neuromuscular Disorders · 1
Implementing a Tiered Genetic Testing Strategy for Muscular Dystrophies in Morocco: From Targeted Assays to Exome Sequencing
2026 · Yasmina Rahmuni, Ilham Ratbi, et al. · Molecular Genetics & Genomic Medicine
Maternally Derived Complex Small Supernumerary Marker Chromosome 22 Associated with Cat-Eye Syndrome Like Features
2025 · Hicham Bouchahta, Zhour EL Amrani, et al. · OBM Genetics
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Unique Female Patient with de novo 6q22.31q27 Duplication and Xq28 Deletion: Case Report and Brief Literature Review
2024 · Lamiae Afif, Zhour El Amrani, et al. · OBM Genetics
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A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature
2024 · Fatima Ouboukss, Zhour El Amrani, et al. · Frontiers in Genetics
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Works count: 32
Citation count: 607
H-index: 10
I10-index: 10
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