about
A Novel Pathogenic Variant in the MITF Gene Segregating with a Unique Spectrum of Ocular Findings in an Extended Iranian Waardenburg Syndrome Kindred.A novel mutation in the PAX3 gene causes Waardenburg syndrome type I in an Iranian family.Cytokine gene polymorphism and graft-versus-host disease: a survey in Iranian bone marrow transplanted patients.Molecular and clinical characterization of Waardenburg syndrome type I in an Iranian cohort with two novel PAX3 mutations.SOX10 mutation causes Waardenburg syndrome associated with distinctive phenotypic features in an Iranian family: A clue for phenotype-directed genetic analysis.Polymorphisms of RPS6KB1 and CD86 associates with susceptibility to multiple sclerosis in Iranian population.Association of P1635 and P1655 polymorphisms in dysbindin (DTNBP1) gene with schizophrenia.
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Q38687462-62EAE06F-5927-40D0-A0D6-DA25208D6E30Q40637334-CE6B9A57-67EC-4D27-8878-B859B890EA4CQ43441667-8F5540EE-F651-47E0-9F3B-496A7FD22A99Q43548321-D3F51818-81F0-4CBA-B372-2CAC562F1E5AQ50180513-F16B5B38-D5E6-4B27-AE4F-6C3D44BB2B7AQ51197012-62E76C6C-E07F-40FD-ABBF-BAFCAD789706Q58898363-B63165B3-C21C-46ED-BCA3-DB5E1C81056D
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Nazanin Jalilian
@ast
Nazanin Jalilian
@en
Nazanin Jalilian
@es
Nazanin Jalilian
@nl
Nazanin Jalilian
@sl
type
label
Nazanin Jalilian
@ast
Nazanin Jalilian
@en
Nazanin Jalilian
@es
Nazanin Jalilian
@nl
Nazanin Jalilian
@sl
prefLabel
Nazanin Jalilian
@ast
Nazanin Jalilian
@en
Nazanin Jalilian
@es
Nazanin Jalilian
@nl
Nazanin Jalilian
@sl
P1053
K-1646-2017
P106
P1153
36113552600
P31
P3829
P496
0000-0002-0361-0096