Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without 'hairy elbows': expanding the phenotype of Wiedemann-Steiner syndrome.
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| Description | scientific article published in December 2015 |
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author: Anu Bashamboo Vincenzo Salpietro Dora Steel Kenneth McElreavey |
| Publication date | December 1, 2015 |
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| Missing/wrong data? | Edit Wikidata item |