Corrigendum: 1q21.1 deletion and a rare functional...

Molecular Case Studies 2020 / 02 Vol. 6; Iss. 1

Corrigendum: 1q21.1 deletion and a rare functional polymorphism in siblings with thrombocytopenia-absent radius–like phenotypes

Brodie, Seth A., Rodriguez-Aulet, Jean Paul, Giri, Neelam, Dai, Jieqiong, Steinberg, Mia, J. Waterfall, Joshua, Roberson, David, Ballew, Bari J., Zhou, Weiyin, Anzick, Sarah L., Jiang, Yuan, Wang, Yon
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Volume:
6
Journal:
Molecular Case Studies
DOI:
10.1101/mcs.a005116
Date:
February, 2020
File:
PDF, 132 KB
2020
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