Detalhe da pesquisa
1.
Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients.
Clin Genet
; 105(6): 611-619, 2024 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-38308583
2.
Genetic Analysis of 27 Y-STR Haplotypes in 11 Iranian Ethnic Groups.
Arch Iran Med
; 27(2): 79-88, 2024 Feb 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38619031
3.
An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene.
Arch Iran Med
; 26(3): 176-180, 2023 03 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37543941
4.
Emerging Epidemiological Data on Rare Intellectual Disability Syndromes from Analyzing the Data of a Large Iranian Cohort.
Arch Iran Med
; 26(4): 186-197, 2023 Apr 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38301078
5.
Implementation of an In-House Platform for Rapid Screening of SARS-CoV-2 Genome Variations.
Arch Iran Med
; 26(2): 69-75, 2023 02 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37543926
6.
Disease Waves of SARS-CoV-2 in Iran Closely Mirror Global Pandemic Trends.
Arch Iran Med
; 25(8): 508-522, 2022 08 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37543873
7.
Novel Mutation in LARP7 in Two Iranian Consanguineous Families with Syndromic Intellectual Disability and Facial Dysmorphism.
Arch Iran Med
; 23(12): 842-847, 2020 12 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33356342