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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...
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| Publié dans: | Expert Rev Mol Med |
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| Auteurs principaux: | , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2005
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| Sujets: | |
| Accès en ligne: | 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 |
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