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 |
---|---|
2012 | 1 |
2015 | 1 |
2022 | 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
Clinical and Genetic Aspects of Phelan-McDermid Syndrome: An Interdisciplinary Approach to Management.
Genes (Basel). 2022 Mar 12;13(3):504. doi: 10.3390/genes13030504.
Genes (Basel). 2022.
PMID: 35328058
Free PMC article.
Review.
[Metatropic dysplasia in a girl with c.1811_1812delinsAT mutation in exon 11 of the TRPV4 gene not previously reported].
Cammarata-Scalisi F, Matysiak-Scholze U, Heinze J, Barrera A, Lacruz-Rengel MA, Bracho A, Guerrero Y.
Cammarata-Scalisi F, et al. Among authors: lacruz rengel ma.
Arch Argent Pediatr. 2015 Jan;113(1):e10-3. doi: 10.5546/aap.2015.e10.
Arch Argent Pediatr. 2015.
PMID: 25622169
Free article.
Spanish.
Item in Clipboard
[Clinical and molecular study of the Noonan syndrome].
Cammarata-Scalisi F, Neri G, Pomponi MG, Mancano G, Da Silva G, Avendaño A, Lacruz-Rengel MA, Stock F, Sosa A.
Cammarata-Scalisi F, et al. Among authors: lacruz rengel ma.
Invest Clin. 2012 Dec;53(4):395-401.
Invest Clin. 2012.
PMID: 23513489
Spanish.
Item in Clipboard
Cite
Cite