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Czech family confirms the new 1p36.13-1p36.12 microdeletion syndrome and the involvement of the critical region with UBR4 and CAPZB genes

Vlasta Cejnova,Pavel Seeman,Sarka Cerna,Ladislava Rennerova,Marie Trkova,Jana Lastuvkova

EUROPEAN JOURNAL OF HUMAN GENETICS（2023）

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