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1.
Regulatory Mutation Study in Cases with Unsolved Hypochromic Microcytic Anemia and α-Major Regulatory Element Haplotype Analysis in Iran.
Hemoglobin
; 45(1): 37-40, 2021 Jan.
Article
in English
| MEDLINE | ID: mdl-33775199
2.
Identification of a novel mutation in the ST14 gene in an Iranian family with ichthyosis and hypotrichosis.
Dermatol Online J
; 25(3)2019 Mar 15.
Article
in English
| MEDLINE | ID: mdl-30982314
3.
Characterization of Niemann-Pick diseases genes mutation spectrum in Iran and identification of a novel mutation in SMPD1 gene.
Med J Islam Repub Iran
; 33: 126, 2019.
Article
in English
| MEDLINE | ID: mdl-32280632
4.
Genetic study of the PAH locus in the Iranian population: familial gene mutations and minihaplotypes.
Metab Brain Dis
; 32(5): 1685-1691, 2017 10.
Article
in English
| MEDLINE | ID: mdl-28676969
5.
Inhibition of breast cancer cell growth and migration through siRNA-mediated modulation of circ_0009910/miR-145-5p/MUC1 axis.
Noncoding RNA Res
; 9(2): 367-375, 2024 Jun.
Article
in English
| MEDLINE | ID: mdl-38511058
6.
MicroRNA biosensors for detection of glioblastoma.
Clin Chim Acta
; 556: 117829, 2024 Mar 15.
Article
in English
| MEDLINE | ID: mdl-38355000
7.
Multi affected pedigree with congenital microcephaly: WES revealed PNKP gene mutation.
Brain Dev
; 41(2): 182-186, 2019 Feb.
Article
in English
| MEDLINE | ID: mdl-30195441
8.
Targeted next generation sequencing identified a novel mutation in MYO7A causing Usher syndrome type 1 in an Iranian consanguineous pedigree.
Int J Pediatr Otorhinolaryngol
; 104: 10-13, 2018 Jan.
Article
in English
| MEDLINE | ID: mdl-29287847
9.
Identification of a Novel Mutation in the PAH Gene in an Iranian Phenylketonuria Family: A Case Report.
Iran J Public Health
; 46(4): 560-564, 2017 Apr.
Article
in English
| MEDLINE | ID: mdl-28540274
10.
A Novel Variant in the PAH Gene Causing Phenylketonuria in an Iranian Pedigree.
Avicenna J Med Biotechnol
; 9(3): 146-149, 2017.
Article
in English
| MEDLINE | ID: mdl-28706611
11.
The spectrum of Familial Mediterranean Fever gene (MEFV) mutations and genotypes in Iran, and report of a novel missense variant (R204H).
Eur J Med Genet
; 60(12): 701-705, 2017 Dec.
Article
in English
| MEDLINE | ID: mdl-28943464
12.
An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria.
Cell J
; 18(2): 229-36, 2016.
Article
in English
| MEDLINE | ID: mdl-27540528
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