Cytogenetic assessment of Fanconi anemia in children with aplastic anemia in Tunisia

Autor: Faten, Talmoudi, Lobna, Kammoun, Nizar, Benhalim, Lamia, Torjemane, Monia, Ouederni, Lamia, Aissaoui, Amel, Lakhal, Fethi, Mellouli, Tarek B, Othmen, Mohamed, Bejaoui, Sonia, Abdelhak, Mounira, Meddeb, Koussay, Dellagi, Sondes, Hdiji, Ahlem, Amouri, S, Hmida

Publikováno v: Journal of Pediatric Hematology/Oncology
Journal of Pediatric Hematology/Oncology, Lippincott, Williams & Wilkins, 2013, 35 (7), pp.547-550. ⟨10.1097/MPH.0b013e31827e56cb⟩

International audience; Background:Chromosome breakage hypersensitivity to alkylating agents is the gold standard test for Fanconi anemia (FA) diagnosis. The aim of the present study was to assess the proportion of FA cases among aplastic anemia (AA)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78ae5a9f6c23b4dbe73c6163bac3598a
https://pubmed.ncbi.nlm.nih.gov/23337544