p16(MTS1/CDK41) mutations and concomitant loss of heterozygosity at 9p21-23 are frequent events in squamous cell carcinoma of the larynx

1. Jares, P.
2. Fernández, P.L.
3. Nadal, A.
4. Cazorla, M.
5. Hernández, L.
6. Pinyol, M.
7. Hernández, S.
8. Traserra, J.
9. Cardesa, A.
10. Campo, E.