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pro vyhledávání: '"Imene Chemkhi"'
Autor:
Helmi Guermani, Imene Chemkhi, Lamia Aissaoui, Lamia Torjmane, Faten Talmoudi, Olfa Kilani, Nabila Abidli, Lobna Kammoun, Neila Ben Romdhane, Tarek Ben Othmane, Nizar Ben Halim, Fethi Mellouli, Wiem Ayed, Moez Elloumi, Sondes Hadiji, Yosra Ben Youssef, Sonia Abdelhak, Ahlem Amouri, Mohamed Bejaoui, Sofiene Hentati
Publikováno v:
Comptes Rendus Biologies
Comptes Rendus Biologies, Elsevier, 2013, 336 (1), pp.29-33. ⟨10.1016/j.crvi.2013.02.001⟩
Comptes Rendus Biologies, Elsevier, 2013, 336 (1), pp.29-33. ⟨10.1016/j.crvi.2013.02.001⟩
International audience; Fanconi anemia (FA) is a recessive chromosomal instability syndrome that is clinically characterized by multiple symptoms. Chromosome breakage hypersensitivity to alkylating agents is the gold standard test for FA diagnosis. I