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To identify candidate regions from larger and multiple lost areas observed from direct tumor studies, the technique of monochromosome transfer was utilized to provide functional evidence to verify and define these deletion findings. An intact chromosome 13 was transferred into the NPC HONE1 cell line. Resultant hybrids were used to map putative TSG activity. A critical region at 13q12 was non\u2010randomly eliminated in all surviving microcell hybrids around the marker D13S893; these hybrids were uniformly tumorigenic. Although a known TSG, <jats:italic>BRCA2<\/jats:italic>, is mapped close to this critical region, no aberrant expression of this gene was detected in microcell hybrids and other NPC cell lines. These results suggest that at least one novel growth control gene on chromosome 13q12, which is not the <jats:italic>BRCA2<\/jats:italic> gene, is essential for hybrid selection and may play a critical role in tumorigenicity. \u00a9 2004 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ijc.11704","type":"journal-article","created":{"date-parts":[[2004,2,9]],"date-time":"2004-02-09T18:27:44Z","timestamp":1076351264000},"page":"357-362","source":"Crossref","is-referenced-by-count":11,"title":["Chromosome 13q12 region critical for the viability and growth of nasopharyngeal carcinoma hybrids"],"prefix":"10.1002","volume":"109","author":[{"given":"Yue","family":"Cheng","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hong Lok","family":"Lung","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Po 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