Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 1 |
2020 | 2 |
2021 | 1 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Reversion to Normal of FMR1 Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families.
Genes (Basel). 2020 Feb 26;11(3):248. doi: 10.3390/genes11030248.
Genes (Basel). 2020.
PMID: 32111011
Free PMC article.
Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double Diagnosis.
Tabolacci E, Pomponi MG, Remondini L, Pietrobono R, Orteschi D, Nobile V, Pucci C, Musto E, Pane M, Mercuri EM, Neri G, Genuardi M, Chiurazzi P, Zollino M.
Tabolacci E, et al. Among authors: remondini l.
Genes (Basel). 2021 Nov 27;12(12):1909. doi: 10.3390/genes12121909.
Genes (Basel). 2021.
PMID: 34946857
Free PMC article.
Item in Clipboard
Methylated premutation of the FMR1 gene in three sisters: correlating CGG expansion and epigenetic inactivation.
Tabolacci E, Pomponi MG, Remondini L, Pietrobono R, Nobile V, Pennacchio G, Gurrieri F, Neri G, Genuardi M, Chiurazzi P.
Tabolacci E, et al. Among authors: remondini l.
Eur J Hum Genet. 2020 May;28(5):567-575. doi: 10.1038/s41431-019-0554-7. Epub 2019 Dec 5.
Eur J Hum Genet. 2020.
PMID: 31804632
Free PMC article.
Item in Clipboard
Cite
Cite