Associated Papers
Identification of Three Novel Mutations in the FANCA, FANCC, and ITGA2B Genes by Whole Exome Sequencing.
Negahdari S et al.
International Journal of Preventive Medicine, 2020
Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; reporting novel and recurrent mutations.
Zafarghandi Motlagh F et al.
Orphanet Journal of Rare Diseases, 2019
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