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
3 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Publication Date timeline is not available.
Page 1
Duplications of SLC1A3: Associated with ADHD and autism.
Eur J Med Genet. 2016 Aug;59(8):373-6. doi: 10.1016/j.ejmg.2016.06.003. Epub 2016 Jun 11.
Eur J Med Genet. 2016.
PMID: 27296938
Quantification of Phenotype Information Aids the Identification of Novel Disease Genes.
Vulto-van Silfhout AT, Gilissen C, Goeman JJ, Jansen S, van Amen-Hellebrekers CJM, van Bon BWM, Koolen DA, Sistermans EA, Brunner HG, de Brouwer APM, de Vries BBA.
Vulto-van Silfhout AT, et al. Among authors: van amen hellebrekers cjm.
Hum Mutat. 2017 May;38(5):594-599. doi: 10.1002/humu.23176. Epub 2017 Feb 2.
Hum Mutat. 2017.
PMID: 28074630
Item in Clipboard
Biallelicframeshift mutation in RIN2 in a patient with intellectual disability and cataract, without RIN2 syndrome.
van Amen-Hellebrekers CJM, Jansen S, Stegmann APA, Stevens SJC, Pfundt R, de Vries BBA.
van Amen-Hellebrekers CJM, et al.
Am J Med Genet A. 2017 Dec;173(12):3238-3240. doi: 10.1002/ajmg.a.38396. Epub 2017 Oct 19.
Am J Med Genet A. 2017.
PMID: 29048725
No abstract available.
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.