p16MTS1/CDK4I mutations and concomitant loss of heterozygosity at 9p21-23 are frequent events in squamous cell carcinoma of the larynx
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E. Campo | P. Jares | M. Pinyol | L. Hernández | A. Nadal | A. Cardesa | M. Cazorla | J. Traserra | P. Fernández | S. Hernández