Clinical heterogeneity and chromosome breakage in Iranian patients suspicious of Fanconi anemia

Clinical heterogeneity and chromosome breakage in Iranian patients suspicious of Fanconi anemia

Background: Fanconi anemia (FA) is a rare autosomal recessive disorder characterized by short stature, skeletal anomalies, increased incidence of solid tumors and leukemia, and bone marrow failure (aplastic anemia). FA has been reported in all races and ethnic groups and affects men and women in an...

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Bibliographic Details
Main Authors: Ghasemi Firoozabadi S, Shafeghati Y, Keyhani E, Kariminejad R, Oloomi Z, Moosavi F, Amini F, Najmabadi H, Behiati F
Format: Article
Language:fas
Published: Tehran University of Medical Sciences 2007-10-01
Series:Tehran University Medical Journal
Subjects:
Fanconi anemia
chromosome breakage
mitomycin c
clinical heterogeneity
Online Access:http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/4218.pdf&manuscript_id=4218

Internet

http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/4218.pdf&manuscript_id=4218

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