The susceptibility gene for familial nasopharyngeal carcinoma is mapped on chromosome 4p11-p14 by haplotype analyses

Chinese Science Bulletin

Volumn 48, Issue 21, 2003, Pages 2327-2330

  Hankui, Chen ^a   Bingjian, Feng ^a   Hui, Liang ^a   Ruhua, Zhang ^a   Yixin, Zeng ^a  

^a SUN YAT SEN UNIVERSITY   (China)

Author keywords

Chromosome 4p11 p1 4; Haplotype analyses; Nasopharyngeal carcinoma; Tumor susceptibility gene

Indexed keywords

EID: 31544433746     PISSN: 10016538     EISSN: 18619541     Source Type: Journal    
DOI: 10.1360/03wc0298     Document Type: Article

References (11)

1. Lu, S. J., Day, N. E., Degos, L. et al., Linkage of a nasopharyngeal carcinoma susceptibility locus to the HLA region. Nature, 1990, 346: 470-471.
2. Feng, B. J., Huang, W., Shugart, Y. Y. et al., Genome-wide scan for familial nasopharyngeal carcinoma and evidence for linkage to chromosome 4, Nat. Genet., 2002, 31: 395-399.
3. Beghini, A., Tibiletti, M., Roversi, G. et al., Germline mutation in the juxtamembrane domain of the KIT gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa, Cancer, 2001, 92: 657-662.
4. Walter, J. W., North, P. E., Waner, M. et al., Somatic mutation of vascular endothelial growth factor receptors in juvenile hemangioma, Genes Chromosomes Cancer, 2002, 33: 295-303.
5. Heinrich, M. C., Corless, C. L., Duensing, A. et al., PDGFRA activating mutations in gastrointestinal stromal tumors. Science, 2003, 299: 708-710.
6. Asanoma, K., Matsuda, T., Kondo, H. et al., NECC1, a candidate choriocarcinoma suppressor gene that encodes a homeodomain consensus motif small star, filled, Genomics, 2003, 81: 15-25.
7. Xi, H.F., Ke, Y.H., Xiao, J.H. et al., Linkage analysis on chromosome 2 in essential hypotension pedigrees. Chin. Sci. Bull., 47(18): 1538-1540.
8. Tan, W., Wu, J.X., Tang, H.J. et al., Expression of cytochrome P450 2E1 in human liver: Relationship between genotype and phenotype in Chinese, Science in China, Ser. C, 2001, 44(4): 356-364.
9. Emahazion, T., Feuk, L., Jobs, M. et al., SNP association studies in Alzheimer's disease highlight problems for complex disease analysis, Trends Genet., 2001, 17(7): 407-13.
10. Collins, F. S., Brooks, L. D., Chakravarti, A., A DNA polymorphism discovery resource for research on human genetic variation. Genome Res., 1998, 8: 1229-1231.
11. Sachidanandam, R., Weissman, D., Schmidt S. C. et al., Map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature, 2001, 409: 928-933.