Publications by authors named "Aziza Sbiti"

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Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report.
Zhour El Amrani, Abdelhafid Natiq, Aziza Sbiti, Ilham Ratbi, Thomas Liehr

Mol Syndromol· March 2024

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A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature.
Fatima Ouboukss, Zhour El Amrani, Hicham Bouchahta, Ilham Ratbi, Aziza Sbiti

Front Genet· February 2024

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Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability.
Zhour El Amrani, Siham Chafai Elalaoui, Wafae Jdioui, Aziza Sbiti, Ilham Ratbi

Ophthalmic Genet· October 2022

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Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemia.
Yassamine Doubaj, Abdelali Zrhidri, Siham Chafai Elalaoui, Jaber Lyahyai, Youssef El Kadiri, Aziza Sbiti

Pan Afr Med J· September 2021

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15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review.
Yahya Benbouchta, Nicole De Leeuw, Saadia Amasdl, Aziza Sbiti, Dominique Smeets

Ital J Pediatr· September 2021

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Molecular diagnosis of dystrophinopathies in Morocco and report of six novel mutations.
Youssef El Kadiri, Yassir Selouani, Ilham Ratbi, Jaber Lyahyai, Abdelali Zrhidri, Aziza Sbiti

Clin Chim Acta· July 2020

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Familial X/Y Translocation Encompassing ARSE in Two Moroccan Siblings with Sensorineural Deafness.
Saadia Amasdl, Wiam Smaili, Abdelhafid Natiq, Amale Hassani, Aziza Sbiti

Cytogenet Genome Res· February 2018

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Cytogenetic Investigation in a Group of Ten Infertile Men with Non-Obstructive Azoospermia: First Algerian 46, XX Syndrome.
Meriem Baziz, Zohra Hamouli-Said, Ilham Ratbi, Mohamed Habel, Soukaina Guaoua, Aziza Sbiti

Iran J Public Health· June 2016

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Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report.
Saadia Amasdl, Abdelhafid Natiq, Siham Chafai Elalaoui, Aziza Sbiti, Thomas Liehr

J Med Case Rep· May 2016

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20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature.
Saadia Amasdl, Abdelhafid Natiq, Aziza Sbiti, Maria Zerkaoui, Jaber Lyahyai

BMC Res Notes· January 2016

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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.
Fatiha El Kerch, Ilham Ratbi, Aziza Sbiti, Fatima-Zohra Laarabi, Amina Barkat

Genet Test Mol Biomarkers· April 2014

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Cytogenetic analysis of 5572 patients referred for suspected chromosomal abnormalities in Morocco.
Nisrine Aboussair, Imane Cherkaoui Jaouad, Souad Cherkaoui Dequaqui, Aziza Sbiti, Fatiha Elkerch

Genet Test Mol Biomarkers· June 2012

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Spinal muscular atrophy carrier frequency and estimated prevalence of the disease in Moroccan newborns.
Jaber Lyahyai, Aziza Sbiti, Amina Barkat, Ilham Ratbi, Abdelaziz Sefiani

Genet Test Mol Biomarkers· March 2012

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Unexpected fertility and paternal UPD 22.
Karim Ouldim, Aziza Sbiti, Abdelbafid Natiq, Fatiha El-Kerch, Souad Cherkaoui

Fertil Steril· November 2008

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Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis.
Lekbir Baala, Sylvain Briault, Heather C Etchevers, Frédéric Laumonnier, Abdelhafid Natiq, Aziza Sbiti

Nat Genet· April 2007

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Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients.
Aziza Sbiti, Fatiha El Kerch, Abdelaziz Sefiani

J Biomed Biotechnol· January 2002

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