Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses.

Source:http://linkedlifedata.com/resource/pubmed/id/9677057

Am. J. Med. Genet. 1998 Jul 7 78 3 237-41

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PMID
9677057