Detalhe da pesquisa
1.
Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families.
J Clin Lab Anal
; 36(2): e24241, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-35019165
2.
Copy number variation analysis implicates novel pathways in patients with oculo-auriculo-vertebral-spectrum and congenital heart defects.
Clin Genet
; 100(3): 268-279, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33988253
3.
Martsolf syndrome with novel mutation in the TBC1D20 gene in a family from Iran.
Am J Med Genet A
; 182(5): 957-961, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32162791
4.
Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect.
Hum Mutat
; 39(10): 1428-1441, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30007050
5.
A comprehensive bioinformatics analysis to identify potential prognostic biomarkers among CC and CXC chemokines in breast cancer.
Sci Rep
; 12(1): 10374, 2022 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35725915
6.
Comparative analysis of protein-protein interaction networks in metastatic breast cancer.
PLoS One
; 17(1): e0260584, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35045088
7.
Integration of gene expression data identifies key genes and pathways in colorectal cancer.
Med Oncol
; 38(1): 7, 2021 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33411100
8.
A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II).
Front Pediatr
; 8: 340, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32671003
9.
The Global Emergency of Novel Coronavirus (SARS-CoV-2): An Update of the Current Status and Forecasting.
Int J Environ Res Public Health
; 17(16)2020 08 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32764417
10.
Prevalence, Type, and Molecular Spectrum of NF1 Mutations in Patients with Neurofibromatosis Type 1 and Congenital Heart Disease.
Genes (Basel)
; 10(9)2019 09 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31487937