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어퍼트 및 크루즌 증후군을 유발하는 골조직 특이성 FGFR2 돌연변이에 의한 두개안면 형태의 변화

Craniofacial morphologic alteration induced by bone-targeted mutants of FGFR2 causing Apert and Crouzon syndrome

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참고문헌

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초록

-어퍼트 및 크루즌 증후군을 유발하는 골조직 특이성 FGFR2 돌연변이에 의한 두개안면 형태의 변화

참고문헌 (41)

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  8. "Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome", 8, pp.98~103 (1994)
  9. "Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome", 9, pp.165~172 (1995)
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  39. "Receptor specificity of the fibroblast growth factor family", 271, pp.15292~15297 (1996)
  40. "Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome", 97, pp.14536~14541 (2000)
  41. "Maxillary growth following LeFort III advancement surgery in Crouzon, Apert, and Pfeiffer syndromes", 90, pp.420~430 (1986)

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