Nouri, Nayereh, Molecular Genetics Laboratory, Alzahra Hospital, Isfahan University of Medical Sciences, Isfahan, Iran

• Vol 17, No 3 (2012) - Case Reports
  A case report of 22q11 deletion syndrome confirmed by array-CGH method
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• Vol 18 (2013): March (Special Issue): Neurology and Neuroscience - Original Article
  Mutation analysis of CACNA1A gene in Iranian migrainous and review literatures
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