Pfeiffer syndrome type 2 associated with a single amino acid deletion in the FGFR2 gene.

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Priolo M, Lerone M, Baffico M, Baldi M, Ravazzolo R, Cama A, Capra V, Silengo M

Pfeiffer syndrome type 2 associated with a single amino acid deletion in the FGFR2 gene.

Clin Genet. 2000 Jul;58(1):81-3.

PubMed ID
10945669 [ View in PubMed
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Polypeptides
NameUniProt ID
Fibroblast growth factor receptor 2P21802Details