Search Page
Save citations to file
Email citations
Email address has not been verified. Go to
My NCBI account settings
to confirm your email and then refresh this page.
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 |
|---|---|
| 1990 | 1 |
| 1996 | 1 |
| 1997 | 1 |
| 2025 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
Failure to detect connexin43 mutations in 38 cases of sporadic and familial heterotaxy.
Circulation. 1996 Oct 15;94(8):1909-12. doi: 10.1161/01.cir.94.8.1909.
Circulation. 1996.
PMID: 8873667
Molecular characterization and functional expression of the human cardiac gap junction channel.
Fishman GI, Spray DC, Leinwand LA.
Fishman GI, et al.
J Cell Biol. 1990 Aug;111(2):589-98. doi: 10.1083/jcb.111.2.589.
J Cell Biol. 1990.
PMID: 1696265
Free PMC article.
Item in Clipboard
Absence of mutations in the regulatory domain of the gap junction protein connexin 43 in patients with visceroatrial heterotaxy.
Penman Splitt M, Tsai MY, Burn J, Goodship JA.
Penman Splitt M, et al.
Heart. 1997 Apr;77(4):369-70. doi: 10.1136/hrt.77.4.369.
Heart. 1997.
PMID: 9155619
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.