Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome
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| Description | scientific article |
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author: Stephen W. Scherer Tracy Stockley Richard F Wintle Sergio L Pereira Muhammad Abu-Elmagd |
| Publication date | January 15, 2015 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |