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Evaluation of Prevalence and Characteristics of Patients with Fanconi Anemia: A Study in Northeast of Iran

Background and objectives: Fanconi anemia (FA) is an autosomal recessive disorder that usually manifest in forms of pancytopenia, hyperpigmentation, and skeletal complications. Mutation in the DNA repair regulatory genes is associated with the development of FA. Examination of chromosomal breakages...

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Principais autores: Sepideh Shakeri, Narjes Soltani, Mohammad Reza Javan, mehrnaz abdolalian, Hossein Ayatollahi, fatemeh shams
Formato: Artigo
Idioma:Inglês
Publicado em: Golestan University of Medical Sciences 2023-01-01
coleção:Medical Laboratory Journal
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Acesso em linha:http://mlj.goums.ac.ir/article-1-1383-en.html
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