Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes
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| Description | scientific article published on 13 October 2016 |
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author: Ricardo D Coletta Breno Rocha Hercílio Martelli Junior Daniela Iancu |
| Publication date | October 13, 2016 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |