FGFR2 mutations in Pfeiffer syndrome
- PMID: 7719333
- DOI: 10.1038/ng0295-108
FGFR2 mutations in Pfeiffer syndrome
Comment in
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Craniofacial syndromes: no such thing as a single gene disease.Nat Genet. 1995 Feb;9(2):101-3. doi: 10.1038/ng0295-101. Nat Genet. 1995. PMID: 7719329 No abstract available.
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