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 |
2013 | 2 |
2014 | 1 |
2019 | 1 |
2023 | 1 |
2024 | 1 |
Search Results
4 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
Cohesin complex-associated holoprosencephaly.
Brain. 2019 Sep 1;142(9):2631-2643. doi: 10.1093/brain/awz210.
Brain. 2019.
PMID: 31334757
Free PMC article.
De novo variants in KCNA3 cause developmental and epileptic encephalopathy.
Soldovieri MV, Ambrosino P, Mosca I, Servettini I, Pietrunti F, Belperio G; KCNA3 study group; Syrbe S, Taglialatela M, Lemke JR.
Soldovieri MV, et al.
Ann Neurol. 2024 Feb;95(2):365-376. doi: 10.1002/ana.26826. Epub 2023 Dec 28.
Ann Neurol. 2024.
PMID: 37964487
Item in Clipboard
Clinical utility of the X-chromosome array.
Zarate YA, Dwivedi A, Bartel FO, Bellomo MA, Cathey SS, Champaigne NL, Clarkson LK, Dupont BR, Everman DB, Geer JS, Gordon BC, Lichty AW, Lyons MJ, Rogers RC, Saul RA, Schroer RJ, Skinner SA, Stevenson RE.
Zarate YA, et al. Among authors: lichty aw.
Am J Med Genet A. 2013 Jan;161A(1):120-30. doi: 10.1002/ajmg.a.35698. Epub 2012 Dec 3.
Am J Med Genet A. 2013.
PMID: 23208842
Item in Clipboard
Unique cerebrovascular anomalies in Noonan syndrome with RAF1 mutation.
Zarate YA, Lichty AW, Champion KJ, Clarkson LK, Holden KR, Matheus MG.
Zarate YA, et al. Among authors: lichty aw.
J Child Neurol. 2014 Aug;29(8):NP13-7. doi: 10.1177/0883073813492384. Epub 2013 Jul 21.
J Child Neurol. 2014.
PMID: 23877478
Item in Clipboard
Cite
Cite