Gene discovery for Mendelian conditions via social networking: de novo variants in KDM1A cause developmental delay and distinctive facial features
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| Description | scientific article |
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author: Jessica X. Chong Peter Lorentzen Margarita Sifuentes Saenz Karen M Park Holly K Tabor Deborah A Nickerson Anita Rauch |
| Publication date | August 2016 |
| Language | English |
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| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |