A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome (Q35238921)
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Current Data About A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
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(P1476) "A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome" (language: en)
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(P2093) M Muenke
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D M McDonald-McGinn
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K Gaudenz
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L A Whitaker
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S P Bartlett
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R I Markowitz
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N H Robin
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N Nwokoro
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J J Mulvihill
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H W Losken
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J B Mulliken
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A E Guttmacher
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R S Wilroy
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L A Clarke
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G Hollway
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L C Adès
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E A Haan
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J C Mulley
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M M Cohen
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G A Bellus
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C A Francomano
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D M Moloney
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S A Wall
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