P133: A homozygous recurrent in-frame deletion in MED22 causes a novel neurodevelopmental disorder
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| Format: | Article |
| Language: | English |
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Elsevier
2023-01-01
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| Series: | Genetics in Medicine Open |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2949774423001620 |