Detalhe da pesquisa
1.
Study of MYOC Gene Mutation in POAG Patients in Zahedan, Iran.
Clin Lab
; 63(7): 1283-1291, 2017 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28792703
2.
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma.
Hum Mol Genet
; 18(20): 3969-77, 2009 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19656777
3.
SVEP1 as a Genetic Modifier of TEK-Related Primary Congenital Glaucoma.
Invest Ophthalmol Vis Sci
; 61(12): 6, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33027505
4.
Genotyping results of Iranian PCG families suggests one or more PCG locus other than GCL3A, GCL3B, and GCL3C exist.
Mol Vis
; 15: 2155-61, 2009 Oct 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-19898634
5.
Association of CTLA-4 gene polymorphisms -318C/T and +49A/G and Hashimoto's thyroidits in Zahedan, Iran.
Biomed Rep
; 6(1): 108-112, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28123718
6.
Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome.
Mol Neurobiol
; 54(9): 7019-7027, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27796743
7.
Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13.1p13.3 and 10q26.3 Duplications.
Int J Mol Cell Med
; 5(4): 236-245, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-28357200
8.
Vitamin D Receptor Gene Polymorphism and the Risk of Multiple Sclerosis in South Eastern of Iran.
J Mol Neurosci
; 56(3): 572-6, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25854779
9.
Positive association of vitamin D receptor gene variations with multiple sclerosis in South East Iranian population.
Biomed Res Int
; 2015: 427519, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25685788
10.
Association between vitamin D receptor polymorphisms and haplotypes with pulmonary tuberculosis.
Biomed Rep
; 3(2): 189-194, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26075071
11.
Association of polymorphisms and haplotypes in the cytochrome P450 1B1 gene with uterine leiomyoma: A case control study.
Biomed Rep
; 3(2): 201-206, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26075073
12.
Diagnosis of cystathionine beta-synthase deficiency by genetic analysis.
J Neurol Sci
; 347(1-2): 305-9, 2014 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25455305