Description of a clinical case 16p13.3 microdeletion with manifestations of alpha-thalassemia-mental retardation syndrome, identified during the chromosomal microarray (CMA) testing

I. V. Anisimova; I. V. Kanivets

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Anisimova I.V., Kanivets I.V. Description of a clinical case 16p13.3 microdeletion with manifestations of alpha-thalassemia-mental retardation syndrome, identified during the chromosomal microarray (CMA) testing. Medical Genetics. 2015;14(11):50-52. (In Russ.) https://doi.org/10.1234/XXXX-XXXX-2015-11-50-52

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ISSN 2073-7998 (Print)

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