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 |
---|---|
2006 | 2 |
2007 | 1 |
2011 | 1 |
2024 | 0 |
Search Results
4 results
Results by year
Filters applied: . Clear all
Page 1
The relationship between MECP2 mutation type and health status and service use trajectories over time in a Rett syndrome population.
Res Autism Spectr Disord. 2011 Jan;5(1):442-449. doi: 10.1016/j.rasd.2010.06.007.
Res Autism Spectr Disord. 2011.
PMID: 21057653
Free PMC article.
Sleep problems in Rett syndrome.
Young D, Nagarajan L, de Klerk N, Jacoby P, Ellaway C, Leonard H.
Young D, et al.
Brain Dev. 2007 Nov;29(10):609-16. doi: 10.1016/j.braindev.2007.04.001. Epub 2007 May 24.
Brain Dev. 2007.
PMID: 17531413
Free PMC article.
Item in Clipboard
NTNG1 mutations are a rare cause of Rett syndrome.
Archer HL, Evans JC, Millar DS, Thompson PW, Kerr AM, Leonard H, Christodoulou J, Ravine D, Lazarou L, Grove L, Verity C, Whatley SD, Pilz DT, Sampson JR, Clarke AJ.
Archer HL, et al.
Am J Med Genet A. 2006 Apr 1;140(7):691-4. doi: 10.1002/ajmg.a.31133.
Am J Med Genet A. 2006.
PMID: 16502428
Free PMC article.
Item in Clipboard
The association between behavior and genotype in Rett syndrome using the Australian Rett Syndrome Database.
Robertson L, Hall SE, Jacoby P, Ellaway C, de Klerk N, Leonard H.
Robertson L, et al.
Am J Med Genet B Neuropsychiatr Genet. 2006 Mar 5;141B(2):177-83. doi: 10.1002/ajmg.b.30270.
Am J Med Genet B Neuropsychiatr Genet. 2006.
PMID: 16389588
Free PMC article.
Item in Clipboard
Cite
Cite