Home > Archives > Vol 13, No 3 (2023) > Clinical and genetic characteristics of the first Russian patient with a syndrome of craniofacial dysmorphia-deafness-anomalies of the upper limbs, caused by a mutation in the PAX3 gene > PDF

Clinical and genetic characteristics of the first Russian patient with a syndrome of craniofacial dysmorphia-deafness-anomalies of the upper limbs, caused by a mutation in the PAX3 gene - PDF (Russian)

Copyright (c) 2023 Markova T.V., Mavlyukeeva V.V., Ginzburg B.G., Shchagina O.A., Nikitin S.S., Dadali E.L.


This work is licensed under a Creative Commons Attribution 4.0 International License.

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