about
The promise of whole-exome sequencing in medical genetics.Beta thalassemia in 31,734 cases with HBB gene mutations: Pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East.An overview of mutation detection methods in genetic disorders.Next generation sequencing: implications in personalized medicine and pharmacogenomics.PCR-ELISA: a diagnostic assay for identifying Iranian HIV seropositives.Genotype, phenotype and in silico pathogenicity analysis of HEXB mutations: Panel based sequencing for differential diagnosis of gangliosidosis.Pathogenic significance of SCN1A splicing variants causing Dravet syndrome: Improving diagnosis with targeted sequencing for variants by in silico analysis.Genotypic effect of a mutation of the MYBPC3 gene and two phenotypes with different patterns of inheritanceBrown-Vialetto-Van Laere syndrome and Fazio-Londe syndrome: A novel mutation and in silico analyses
P50
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P50
description
researcher
@en
wetenschapper
@nl
name
Bahareh Rabbani
@en
Bahareh Rabbani
@nl
type
label
Bahareh Rabbani
@en
Bahareh Rabbani
@nl
prefLabel
Bahareh Rabbani
@en
Bahareh Rabbani
@nl
P31
P496
0000-0003-1083-1660