Associated Papers
Gorlin Syndrome: Recent Advances in Genetic Testing and Molecular and Cellular Biological Research.
Onodera S et al.
International Journal of Molecular Sciences, 2020
33066274 (PubMed )
Supplement: ijms-21-07559-s001.pdf
Frequency and features of TP53 mutation in 30 Chinese patients with sporadic basal cell carcinoma.
Wang YM et al.
Clinical and Experimental Dermatology, 2014
Unique features of PTCH1 mutation spectrum in Chinese sporadic basal cell carcinoma.
Huang YS et al.
Journal of the European Academy of Dermatology and Venereology : Jeadv, 2013
PTCH1 gene mutations in Keratocystic odontogenic tumors: a study of 43 Chinese patients and a systematic review.
Guo YY et al.
Plos One, 2013
24204797 (PubMed )
Supplement: pone.0077305.s001.docx
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