Detalhe da pesquisa
1.
Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome.
Int J Mol Sci
; 24(11)2023 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37298158
2.
Genotype-Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review.
Genes (Basel)
; 14(2)2023 02 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36833393
3.
Mitochondrial Dysfunction, Oxidative Stress, and Therapeutic Strategies in Diabetes, Obesity, and Cardiovascular Disease.
Antioxidants (Basel)
; 12(3)2023 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36978905
4.
Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype-Phenotype Correlation.
Genes (Basel)
; 13(11)2022 11 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36360320
5.
Genetic Polymorphisms in a Familial Hypercholesterolemia Population from North-Eastern Europe.
J Pers Med
; 12(3)2022 Mar 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35330428