Caricamento...
Prenatal diagnosis in a hereditary Peutz-Jeghers syndrome family with high cancer risk
BACKGROUND: Peutz-Jeghers Syndrome (PJS) is a hereditary cancer predisposing syndrome caused by autosomal dominant mutations in the serine/threonine kinase 11 (STK11) gene and is associated with decreased life expectancy. Many families experience a poorer quality of life due to the psychological bur...
Salvato in:
| Pubblicato in: | BMC Med Genet |
|---|---|
| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2018
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5930790/ https://ncbi.nlm.nih.gov/pubmed/29720104 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-018-0594-9 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|