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P79 Clinical case of rare chromosome pathology: combined deletion 7p21.1-p15.2 and deletion 22q12.1 in patient with mental retardation

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Namazova-Baranova L, Savostyanov K, Vashkamadze N, et al
P79 Clinical case of rare chromosome pathology: combined deletion 7p21.1-p15.2 and deletion 22q12.1 in patient with mental retardation

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  • First published June 6, 2017.
Online issue publication 
June 06, 2017

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