Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?

Author:

Eng C,Murday V,Seal S,Mohammed S,Hodgson S V,Chaudary M A,Fentiman I S,Ponder B A,Eeles R A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference10 articles.

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