On the significance of craniosynostosis in a case of Kabuki syndrome with a concomitant KMT2D mutation and 3.2 Mbp de novo 10q22.3q23.1 deletion.
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| Description | scientific article published on 7 June 2017 |
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author: Alexandra Topa |
| Publication date | June 7, 2017 |
| Language | English |
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