about
A novel homozygous LMNA mutation (p.Met540Ile) causes mandibuloacral dysplasia type A.A new approach for molecular diagnosis of TAR syndrome.First Case Report of EX3del4765 Mutation in PAH Gene in Asian Population.Multidisciplinary management of a patient with van der Woude syndrome: A case report.Mutation spectra of the ITGB2 gene in Iranian families with leukocyte adhesion deficiency type 1.Mutation spectra of the AAAS gene in Iranian families with Allgrove Syndrome.Screening for genomic rearrangements at BRCA1 locus in Iranian women with breast cancer using multiplex ligation-dependent probe amplification.A novel splice site mutation in the GNPTAB gene in an Iranian patient with mucolipidosis II α/β.Novel FKBP10 Mutation in a Patient with Osteogenesis Imperfecta Type XI
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Vahid Reza Yassaee
@ast
Vahid Reza Yassaee
@en
Vahid Reza Yassaee
@es
Vahid Reza Yassaee
@nl
Vahid Reza Yassaee
@sl
type
label
Vahid Reza Yassaee
@ast
Vahid Reza Yassaee
@en
Vahid Reza Yassaee
@es
Vahid Reza Yassaee
@nl
Vahid Reza Yassaee
@sl
prefLabel
Vahid Reza Yassaee
@ast
Vahid Reza Yassaee
@en
Vahid Reza Yassaee
@es
Vahid Reza Yassaee
@nl
Vahid Reza Yassaee
@sl
P1053
G-4086-2017
P106
P31
P3829
P496
0000-0002-1879-3905