Molecular basis of the clinical features of Holt–Oram...

Molecular basis of the clinical features of Holt–Oram syndrome resulting from missense and extended protein mutations of the TBX5 gene as well as TBX5 intragenic duplications

Al-Qattan, Mohammad M., Abou Al-Shaar, Hussam
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Volume:
560
Language:
english
Journal:
Gene
DOI:
10.1016/j.gene.2015.02.017
Date:
April, 2015
File:
PDF, 602 KB
english, 2015
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