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pro vyhledávání: '"Taghavi, Maryam"'
Autor:
Amirian, Azam, Karimipoor, Morteza, Jafarinejad, Masoumeh, Taghavi, Maryam, Kordafshari, Alireza, Fathi Azar, Samaneh, Mohammadi, Malihe Sadat, Zeinali, Sirous
Publikováno v:
Archives of Iranian Medicine
Archives of Iranian Medicine, Academy of Medical Sciences of the I.R. Iran, 2011, 14 (1), pp.8-11
Archives of Iranian Medicine, Academy of Medical Sciences of the I.R. Iran, 2011, 14 (1), pp.8-11
International audience; BACKGROUND: Co-inheritance of β- and δ-globin mutations in Iran is not uncommon. This situation may interfere with correct diagnosis and genetic counseling of α- and β-thalassemia in screening programs. Here we report the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::13e5d7c60e25de31dba3924e51147df5
https://hal-riip.archives-ouvertes.fr/pasteur-00829009/document
https://hal-riip.archives-ouvertes.fr/pasteur-00829009/document