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
Search Results
2 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Publication Date timeline is not available.
Page 1
Modeling Rare Human Disorders in Mice: The Finnish Disease Heritage.
Cells. 2021 Nov 13;10(11):3158. doi: 10.3390/cells10113158.
Cells. 2021.
PMID: 34831381
Free PMC article.
Review.
Loss-of-function mutations of the TIE1 receptor tyrosine kinase cause late-onset primary lymphedema.
Brouillard P, Murtomäki A, Leppänen VM, Hyytiäinen M, Mestre S, Potier L, Boon LM, Revencu N, Greene A, Anisimov A, Salo MH, Hinttala R, Eklund L, Quéré I, Alitalo K, Vikkula M.
Brouillard P, et al. Among authors: salo mh.
J Clin Invest. 2024 May 30;134(14):e173586. doi: 10.1172/JCI173586.
J Clin Invest. 2024.
PMID: 38820174
Free PMC article.
Item in Clipboard
Cite
Cite
ARTICLE TYPE
ARTICLE LANGUAGE
AGE
Filters on the sidebar will be reset to the default list and any currently applied filters will be cleared.