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Axillary basal cell carcinoma: additional 25 patients and considerations

✍ Scribed by R. Betti; C. Crosti; L. Moneghini; E. Crespi; S. Menni


Book ID
111098474
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
94 KB
Volume
25
Category
Article
ISSN
0926-9959

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## Mutations in the PTCH gene, the human homolog of the Drosophila patched gene, have been found to lead to the autosomal dominant disorder termed Nevoid Basal Cell Carcinoma Syndrome (NBCCS, also called Gorlin Syndrome). Patients display an array of developmental anomalies and are prone to develop

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