Germline mutations of the PTCH gene in families with odontogenic keratocysts and nevoid basal cell carcinoma syndrome

Tumor Biology

Volumn 27, Issue 4, 2006, Pages 175-180

  Song, Ya Ling ^a   Zhang, Wen Feng ^a   Peng, Bin ^a   Wang, Chang Ning ^a   Wang, Qing ^b   Bian, Zhuan ^a  

^a WUHAN UNIVERSITY   (China)

^b LERNER RESEARCH INSTITUTE   (United States)

Author keywords

Germline mutation; Nevoid basal cell carcinoma syndrome; Odontogenic keratocyst; PTCH gene

Indexed keywords

DNA;

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BASAL CELL NEVUS SYNDROME; CANCER DIAGNOSIS; CHINESE; CLINICAL ARTICLE; FEMALE; GENE AMPLIFICATION; GENE IDENTIFICATION; GENE ISOLATION; GENE MUTATION; GERM LINE; HUMAN; HUMAN CELL; HUMAN TISSUE; JAW CANCER; MALE; MISSENSE MUTATION; NONSENSE MUTATION; ODONTOGENIC TUMOR; ONCOGENE; PRIORITY JOURNAL; PTCH GENE; SCHOOL CHILD;

EID: 33646734450     PISSN: 10104283     EISSN: None     Source Type: Journal    
DOI: 10.1159/000093054     Document Type: Article

References (21)

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