Jackson-Weiss syndrome: identification of two novel FGFR2 missense mutations shared with Crouzon and Pfeiffer craniosynostotic disorders (Q56380668)

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Jackson-Weiss syndrome: identification of two novel FGFR2 missense mutations shared with Crouzon and Pfeiffer craniosynostotic disorders
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    Jackson-Weiss syndrome: identification of two novel FGFR2 missense mutations shared with Crouzon and Pfeiffer craniosynostotic disorders (English)
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    C Di Rocco
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    E Lajeunie
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    S Valeri
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    F Velardi
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    P A Battaglia
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    November 1997
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    101
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    1
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    47-50
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