ArticleBMC medical genetics2011
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome.
Aimee L Fenwick et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
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ArticleBMC medical genetics2011
Aimee L Fenwick et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.