A novel heterozygous variant in FGF9 associated with previously unreported features of multiple synostosis syndrome 3.
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PMID: 33174625 [PubMed - as supplied by publisher]
Source: Clinical Genetics - Category: Genetics & Stem Cells Authors: Thuresson AC, Croft B, Hailer YD, Liminga G, Arvidsson CG, Harley VR, Stattin EL Tags: Clin Genet Source Type: research