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mutationmicrodeletion9q22.3geneticsScience Articles
Microdeletion of 9q22.3: A patient with minimal deletion size associated with a severe phenotype
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The art of Robert J. Gorlin, DDS, MS
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Basaloid follicular hamartomas in pediatric Basal Cell Nevus Syndrome: A diagnostic challenge Click here to view the article on PubMed.gov
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New Clinical Trial Opportunity
mutationgeneticsScience ArticlesmosaicismSMO
A Novel Case of Gorlin Syndrome Mosaicism Involving an SMO Gene Mutation: Clinical, Histological and Molecular Analysis of Basaloid Tumours
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Multiple basal cell carcinomas in Gorlin Syndrome treated with pulsed dye laser
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Jaunts with Julie
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This survey provides comprehensive information on the challenges the Gorlin syndrome community faces.
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