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"Novel p.C620L RET Mutation Detected in a Patient with Medullary Thyroid Carcinoma"
written by Anatole A. Klyosov, Igor L. Rozhanskii,
published by International Journal of Clinical Medicine, Vol.3 No.6, 2012
has been cited by the following article(s)：
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[1] De novo heterozygous FBN1 mutations in the extreme C‐terminal region cause progeroid fibrillinopathy
American Journal of Medical Genetics Part A 2014 - No relevant information.