Markova T.V., Mavlyukeeva V.V., Ginzburg B.G., Shchagina O.A., Nikitin S.S., Dadali E.L. 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. Neuromuscular Diseases. 2023;13(3):48-53. (In Russ.) https://doi.org/10.17650/2222-8721-2023-13-3-48-53
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