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 |
---|---|
2018 | 2 |
2019 | 1 |
2020 | 1 |
2021 | 2 |
2024 | 0 |
Search Results
5 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
The Cytoscan HD Array in the Diagnosis of Neurodevelopmental Disorders.
High Throughput. 2018 Sep 14;7(3):28. doi: 10.3390/ht7030028.
High Throughput. 2018.
PMID: 30223503
Free PMC article.
Review.
A 46,XY Female with a 9p24.3p24.1 Deletion and a 8q24.11q24.3 Duplication: A Case Report and Review of the Literature.
Bruni V, Roppa K, Scionti F, Apa R, Sestito S, Di Martino MT, Pensabene L, Concolino D.
Bruni V, et al.
Cytogenet Genome Res. 2019;158(2):74-82. doi: 10.1159/000500619. Epub 2019 May 28.
Cytogenet Genome Res. 2019.
PMID: 31141803
Review.
Item in Clipboard
A Psychometric Properties Evaluation of the Italian Version of the Geriatric Depression Scale.
Galeoto G, Sansoni J, Scuccimarri M, Bruni V, De Santis R, Colucci M, Valente D, Tofani M.
Galeoto G, et al. Among authors: bruni v.
Depress Res Treat. 2018 Mar 1;2018:1797536. doi: 10.1155/2018/1797536. eCollection 2018.
Depress Res Treat. 2018.
PMID: 29686898
Free PMC article.
Item in Clipboard
Facial Dysmorphisms, Macrodontia, Focal Epilepsy, and Thinning of the Corpus Callosum: A Rare Mild Form of Kabuki Syndrome.
Bruni V, Scozzafava C, Gnazzo M, Parisi F, Sestito S, Pensabene L, Novelli A, Concolino D.
Bruni V, et al.
J Pediatr Genet. 2021 Mar;10(1):49-52. doi: 10.1055/s-0040-1701645. Epub 2020 Feb 17.
J Pediatr Genet. 2021.
PMID: 33552639
Free PMC article.
Item in Clipboard
A Novel Splicing Variant of COL2A1 in a Fetus with Achondrogenesis Type II: Interpretation of Pathogenicity of In-Frame Deletions.
Bruni V, Spoleti CB, La Barbera A, Dattilo V, Colao E, Votino C, Bellacchio E, Perrotti N, Giglio S, Iuliano R.
Bruni V, et al.
Genes (Basel). 2021 Sep 10;12(9):1395. doi: 10.3390/genes12091395.
Genes (Basel). 2021.
PMID: 34573377
Free PMC article.
Item in Clipboard
Cite
Cite