Concurrent occurrence of an inherited 16p13.11 microduplication and a de novo 19p13.3 microdeletion involving MAP2K2 in a patient with developmental delay, distinctive facial features, and lambdoid synostosis
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| Description | scientific article published on 14 October 2016 |
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author: Toshiyuki Yamamoto |
| Publication date | October 14, 2016 |
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