(Q28304096)

English

Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome

scientific article

Statements

Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome (English)
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U Schell
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A Hehr
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G J Feldman
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N H Robin
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E H Zackai
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C de Die-Smulders
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D H Viskochil
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J M Stewart
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G Wolff
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H Ohashi
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March 1995
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4
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323-8
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3
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Identifiers

 
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