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 |
---|---|
2013 | 2 |
2015 | 1 |
2016 | 1 |
2019 | 1 |
2020 | 1 |
2021 | 1 |
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
Netrin-G2 dysfunction causes a Rett-like phenotype with areflexia.
Hum Mutat. 2020 Feb;41(2):476-486. doi: 10.1002/humu.23945. Epub 2019 Nov 15.
Hum Mutat. 2020.
PMID: 31692205
Microcephaly-dystonia due to mutated PLEKHG2 with impaired actin polymerization.
Edvardson S, Wang H, Dor T, Atawneh O, Yaacov B, Gartner J, Cinnamon Y, Chen S, Elpeleg O.
Edvardson S, et al. Among authors: atawneh o.
Neurogenetics. 2016 Jan;17(1):25-30. doi: 10.1007/s10048-015-0464-y. Epub 2015 Nov 17.
Neurogenetics. 2016.
PMID: 26573021
Item in Clipboard
Biallelic deletion in a minimal CAPN15 intron in siblings with a recognizable syndrome of congenital malformations and developmental delay.
Mor-Shaked H, Salah S, Yanovsky-Dagan S, Meiner V, Atawneh OM, Abu-Libdeh B, Elpeleg O, Harel T.
Mor-Shaked H, et al. Among authors: atawneh om.
Clin Genet. 2021 Apr;99(4):577-582. doi: 10.1111/cge.13920. Epub 2021 Jan 13.
Clin Genet. 2021.
PMID: 33410501
Item in Clipboard
A congenital neutrophil defect syndrome associated with mutations in VPS45.
Vilboux T, Lev A, Malicdan MC, Simon AJ, Järvinen P, Racek T, Puchalka J, Sood R, Carrington B, Bishop K, Mullikin J, Huizing M, Garty BZ, Eyal E, Wolach B, Gavrieli R, Toren A, Soudack M, Atawneh OM, Babushkin T, Schiby G, Cullinane A, Avivi C, Polak-Charcon S, Barshack I, Amariglio N, Rechavi G, van der Werff ten Bosch J, Anikster Y, Klein C, Gahl WA, Somech R.
Vilboux T, et al. Among authors: atawneh om.
N Engl J Med. 2013 Jul 4;369(1):54-65. doi: 10.1056/NEJMoa1301296. Epub 2013 Jun 5.
N Engl J Med. 2013.
PMID: 23738510
Free PMC article.
Item in Clipboard
West syndrome, microcephaly, grey matter heterotopia and hypoplasia of corpus callosum due to a novel ARFGEF2 mutation.
Banne E, Atawneh O, Henneke M, Brockmann K, Gärtner J, Elpeleg O, Edvardson S.
Banne E, et al. Among authors: atawneh o.
J Med Genet. 2013 Nov;50(11):772-5. doi: 10.1136/jmedgenet-2013-101752. Epub 2013 Jun 28.
J Med Genet. 2013.
PMID: 23812912
Item in Clipboard
Cite
Cite