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Wiley, The American Journal of Medical Genetics - Part A, 5(188), p. 1600-1606, 2022

DOI: 10.1002/ajmg.a.62642

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Refining the clinical phenotype associated with missense variants in exons 38 and 39 of KMT2D

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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