Lataa...
Prader–Willi syndrome: clinical genetics, cytogenetics and molecular biology
Prader–Willi syndrome (PWS) is a neurodevelopmental disorder that arises from lack of expression of paternally inherited genes known to be imprinted and located in the chromosome 15q11-q13 region. PWS is considered the most common syndromal cause of life-threatening obesity and is estimated at 1 in...
Tallennettuna:
| Julkaisussa: | Expert Rev Mol Med |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2005
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6750281/ https://ncbi.nlm.nih.gov/pubmed/16038620 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S1462399405009531 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|