De Novo Alu-Element Insertions in FGFR2 Identify a Distinct Pathological Basis for Apert Syndrome
- 1 February 1999
- journal article
- case report
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (2) , 446-461
- https://doi.org/10.1086/302245
Abstract
No abstract availableKeywords
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