A unique coincidence of a 17q12 deletion and duplication in a Czech family led to a refined genotype-phenotype correlation

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Bibliographic Details
Published in:American journal of medical genetics. Part A 2023, Vol.191 (3), p.870-877
Main Authors: Zunova, Hana, Stolfa, Miroslav, Kunikova, Tereza, Novotna, Drahuse, Valkovicova, Radka, Štěrbová, Katalin, Vlckova, Marketa
Format: Report
Language:English
Online Access:Get full text
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ISSN:1552-4833
DOI:10.1002/ajmg.a.63085