Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemia

INTRODUCTION: Fanconi anemia (FA) is a rare inherited hematological disease due to a defect in the DNA repair pathway resulting in congenital abnormalities and high susceptibility to develop cancers. The cytogenetic analysis using alkylating agents is still a reference test to establish the diagnosi...

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Detalles Bibliográficos
Autores principales: Doubaj, Yassamine, Zrhidri, Abdelali, Elalaoui, Siham Chafai, Lyahyai, Jaber, El Kadiri, Youssef, Elkassimi, Nadia, Sbiti, Aziza, El Kababri, Maria, Hessissen, Laila, Sefiani, Abdelaziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2021
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363957/
https://www.ncbi.nlm.nih.gov/pubmed/34422195
http://dx.doi.org/10.11604/pamj.2021.39.72.27220

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8363957/
https://www.ncbi.nlm.nih.gov/pubmed/34422195
http://dx.doi.org/10.11604/pamj.2021.39.72.27220

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