Wordt geladen...
Prader–Willi syndrome and autism spectrum disorders: an evolving story
Prader–Willi syndrome (PWS) is well-known for its genetic and phenotypic complexities. Caused by a lack of paternally derived imprinted material on chromosome 15q11–q13, individuals with PWS have mild to moderate intellectual disabilities, repetitive and compulsive behaviors, skin picking, tantrums,...
Bewaard in:
| Hoofdauteurs: | , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Springer US
2011
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3261277/ https://ncbi.nlm.nih.gov/pubmed/21858456 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11689-011-9092-5 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|