Related references
Note: Only part of the references are listed.Basal cell naevus syndrome: an update on genetics and treatment
A. M. John et al.
BRITISH JOURNAL OF DERMATOLOGY (2016)
Genomic analysis identifies new drivers and progression pathways in skin basal cell carcinoma
Ximena Bonilla et al.
NATURE GENETICS (2016)
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
Sue Richards et al.
GENETICS IN MEDICINE (2015)
Molecular evidence of type 2 mosaicism in Gorlin syndrome
A. Torrelo et al.
BRITISH JOURNAL OF DERMATOLOGY (2013)
PTCH-ing It Together: A Basal Cell Nevus Syndrome Review
Charlene Lam et al.
DERMATOLOGIC SURGERY (2013)
Consensus Statement From the First International Colloquium on Basal Cell Nevus Syndrome (BCNS)
Alanna F. Bree et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2011)
Mechanisms of Inactivation of PTCH1 Gene in Nevoid Basal Cell Carcinoma Syndrome: Modification of the Two-Hit Hypothesis
Shuang Pan et al.
CLINICAL CANCER RESEARCH (2010)
Nevoid basal cell carcinoma syndrome (Gorlin syndrome)
Lorenzo Lo Muzio
ORPHANET JOURNAL OF RARE DISEASES (2008)
Somatic mutations in the PTCH, SMOH, SUFUH and TP53 genes in sporadic basal cell carcinomas
J Reifenberger et al.
BRITISH JOURNAL OF DERMATOLOGY (2005)
Alternative first exons of PTCH1 are differentially regulated in vivo and may confer different functions to the PTCH1 protein
P Kogerman et al.
ONCOGENE (2002)
Unbalanced overexpression of the mutant allele in murine Patched mutants
J Calzada-Wack et al.
CARCINOGENESIS (2002)