Spectrum of PTCH1 Mutations in French Patients with Gorlin Syndrome

Author:

Boutet Nathalie,Bignon Yves-Jean,Drouin-Garraud Valérie,Sarda Pierre,Longy Michel,Lacombe Didier,Gorry Philippe

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference24 articles.

1. Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome;Aszterbaum;J Invest Dermatol,1998

2. GDNF as a candidate modifier in a type 1 neurofibromatosis (NF1) enteric phenotype;Bahuau;J Med Genet,2001

3. Mutations in the human homologue of the Drosophila patched gene in Caucasian and African-American nevoid basal cell carcinoma syndrome patients;Chidambaram;Cancer Res,1996

4. NF1 microdeletion breakpoints are clustered at flanking repetitive sequences;Dorschner;Hum Mol Genet,2000

5. Complications of the naevoid basal cell carcinoma syndrome: Results of a population based study;Evans;J Med Genet,1993

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