Načítá se...
Early detection of Angelman syndrome resulting from de novo paternal isodisomic 15q UPD and review of comparable cases
BACKGROUND: Angelman syndrome is a rare neurogenetic disorder that results in intellectual and developmental disturbances, seizures, jerky movements and frequent smiling. Angelman syndrome is caused by two genetic disturbances: either genes on the maternally inherited chromosome 15 are deleted or in...
Uloženo v:
| Hlavní autoři: | , , , , , , , , |
|---|---|
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2013
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3846355/ https://ncbi.nlm.nih.gov/pubmed/24011290 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-6-35 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|