Inherited genetic markers for thrombophilia in northeastern Iran (a clinical-based report)

Por Keify, Fatemeh, Azimi-Nezhad, Mohsen, Zhiyan-abed, Narges, Nasseri, Mojila, Abbaszadegan, Mohammad Reza
Publicado no Rep Biochem Mol Biol (2014)

B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype–phenotype associations in the muscular dystrophy-dystroglycan...

Por Maroofian, Reza, Riemersma, Moniek, Jae, Lucas T., Zhianabed, Narges, Willemsen, Marjolein H., Wissink-Lindhout, Willemijn M., Willemsen, Michèl A., de Brouwer, Arjan P. M., Mehrjardi, Mohammad Yahya Vahidi, Ashrafi, Mahmoud Reza, Kusters, Benno, Kleefstra, Tjitske, Jamshidi, Yalda, Nasseri, Mojila, Pfundt, Rolph, Brummelkamp, Thijn R., Abbaszadegan, Mohammad Reza, Lefeber, Dirk J., van Bokhoven, Hans
Publicado no Genome Med (2017)