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1.
Performance of conventional cytogenetic analysis on chorionic villi when only one cell layer, cytotrophoblast or mesenchyme alone, is analyzed.
Prenat Diagn
; 41(6): 652-660, 2021 May.
Article
in English
| MEDLINE | ID: mdl-33782989
2.
Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene.
Hum Genet
; 139(2): 227-245, 2020 Feb.
Article
in English
| MEDLINE | ID: mdl-31919630
3.
Transcriptional Reactivation of the FMR1 Gene. A Possible Approach to the Treatment of the Fragile X Syndrome.
Genes (Basel)
; 7(8)2016 Aug 17.
Article
in English
| MEDLINE | ID: mdl-27548224
4.
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells.
Epigenetics Chromatin
; 9: 12, 2016.
Article
in English
| MEDLINE | ID: mdl-27014370
5.
Defining the role of the CGGBP1 protein in FMR1 gene expression.
Eur J Hum Genet
; 24(5): 697-703, 2016 May.
Article
in English
| MEDLINE | ID: mdl-26306647
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