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pubmed: wnt1
Feed retrieval for pubmed: wnt1 on 10/09/2020, 12:11
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Biallelic INTS1 Mutations Cause a Rare Neurodevelopmental Disorder in Two Chinese Siblings.
https://www.ncbi.nlm.nih.gov/pubmed/31428919?dopt=Abstract
pubmed: wnt1
j