Association of FANCC and PTCH1 with the Development of Early Dysplastic Lesions of the Head and Neck

Author:

Ghosh Amlan,Ghosh Susmita,Maiti Guru Prasad,Mukherjee Sudeshna,Mukherjee Nupur,Chakraborty Jayanta,Roy Anup,Roychoudhury Susanta,Panda C. K.

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Surgery

Reference25 articles.

1. Tripathi A, Dasgupta S, Roy A, et al. Sequential deletions in both arms of chromosome 9 are associated with the development of head and neck squamous cell carcinoma in Indian patients. J Exp Clin Cancer Res. 2003;322:289–97.

2. Ordonez BP, Beauchemin M, Jordan RCK. Molecular biology of squamous cell carcinoma of the head and neck. J Clin Pathol. 2006;59:445–53.

3. Kim MM, Califano JA. Molecular pathology of head and neck cancer. Int J Cancer. 2004;112:545–53.

4. Shao JY, Zeng WF, Zeng YX. Molecular genetic progression on nasopharyngeal carcinoma. Ai Zheng. 2002;21:1–10.

5. Sinha S, Singh R, Alam N, et al. Alterations in candidate genes PHF2, FANCC, PTCH1 and XPA at chromosomal 9q22.3 region: pathological significance in early- and late-onset breast carcinoma. Mol Cancer. 2008;7:84.

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