Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome (Q28304096)
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(P31) (Q13442814)
(P304) 323-8
(P407) (Q1860)
(P433) 3
(P478) 4
(P577) +1995-03-00T00:00:00Z
(P921) (Q1286848)
(P1433) (Q2720965)
(P1476) "Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome" (language: en)
(P2093) U Schell
A Hehr
G J Feldman
N H Robin
E H Zackai
C de Die-Smulders
D H Viskochil
J M Stewart
G Wolff
H Ohashi
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