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1.
Identification of a Novel ARSA Gene Mutation Through High-Throughput Molecular Diagnosis Method in Two Girls with Late Infantile Metachromatic Leukodystrophy.
Neuromolecular Med
; 25(4): 563-572, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-37682448
2.
Clinical and genetic screening in a large Iranian family with Marfan syndrome: A case study.
Health Sci Rep
; 6(10): e1647, 2023 Oct.
Article
in English
| MEDLINE | ID: mdl-37877128
3.
ACAN, MDFI, and CHST1 as Candidate Genes in Gastric Cancer: A Comprehensive Insilco Analysis.
Asian Pac J Cancer Prev
; 23(2): 683-694, 2022 Feb 01.
Article
in English
| MEDLINE | ID: mdl-35225482
4.
Association Between Retinoid X Receptor Gene Variants and Dyslipidemia Risk in an Iranian Population.
Cureus
; 13(9): e17730, 2021 Sep.
Article
in English
| MEDLINE | ID: mdl-34659944
5.
Identification of Balanced and Unbalanced Complex Chromosomal Rearrangement Involving Chromosomes 1, 11, and 15.
Cureus
; 13(7): e16166, 2021 Jul.
Article
in English
| MEDLINE | ID: mdl-34367776
6.
Fragile X Syndrome in a Female With Homozygous Full-Mutation Alleles of the FMR1 Gene.
Cureus
; 13(7): e16340, 2021 Jul.
Article
in English
| MEDLINE | ID: mdl-34395123
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