volume 15, issue 3, P301-306 2016
DOI: 10.15690/vsp.v15i3.1568
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Г. С. Васильев, Т. И. Мещерякова, Е. Н. Лукаш, С. С. Жилина, И. В. Канивец, А. Н. Петрин

Abstract: The article presents a detailed clinical and molecular and cytogenetic analysis of the unique case of a rare chromosomal abnormality (duplication of 14q11.2-q21.1 and deletion of 21q11.2-q21.3