Caricamento...
X-Chromosome Inactivation Patterns in Females With Prader–Willi Syndrome
Prader–Willi syndrome (PWS) is a complex neurodevelopmental disorder caused by loss of paternally expressed genes from the 15q11-q13 region generally due to a paternally-derived deletion of the 15q11-q13 region or maternal disomy 15 (UPD). Maternal disomy 15 is usually caused by maternal meiosis I n...
Salvato in:
| Pubblicato in: | Am J Med Genet A |
|---|---|
| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2007
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5459689/ https://ncbi.nlm.nih.gov/pubmed/17036338 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.31506 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|