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Wiley, Clinical Genetics, 1(95), p. 165-171, 2018

DOI: 10.1111/cge.13458

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Novel exostosin‐2 missense variants in a family with autosomal recessive exostosin‐2‐related syndrome: further evidences on the phenotype

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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