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A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis
A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis
Detailed Information
- Material Type
- 기사
- ISSN
- 87563282
- Author
- Yin, L.
- Title/Author
- A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis / Yin, L. ; 공저 Du, X. ; Li, C. ; Xu, X. ; Chen, Z. ; Su, N. ; Zhao, L. ; Qi, H. ; Li, F. ; Xue, J.
- Publish Info
- Oxford : Elsevier Inc, 2008.
- Material Info
- pp. 631-643
- General Note
- included reference
- Added Entry-Personal Name
- Du, X.
- Added Entry-Personal Name
- Li, C.
- Added Entry-Personal Name
- Xu, X.
- Added Entry-Personal Name
- Chen, Z.
- Added Entry-Personal Name
- Su, N.
- Added Entry-Personal Name
- Zhao, L.
- Added Entry-Personal Name
- Qi, H.
- Added Entry-Personal Name
- Li, F.
- Added Entry-Personal Name
- Xue, J.
- Electronic Location and Access
- url
- 모체레코드
- 모체정보확인
- Control Number
- kjul:60246087
MARC
008191122s2008 ai aa eng■022 ▼a87563282
■1001 ▼aYin, L.
■24510▼aA Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis▼dYin, L.▼e공저 Du, X.▼eLi, C.▼eXu, X.▼eChen, Z.▼eSu, N.▼eZhao, L.▼eQi, H.▼eLi, F.▼eXue, J.
■260 ▼aOxford▼bElsevier Inc▼c2008.
■300 ▼app. 631-643
■500 ▼aincluded reference
■7001 ▼aDu, X.
■7001 ▼aLi, C.
■7001 ▼aXu, X.
■7001 ▼aChen, Z.
■7001 ▼aSu, N.
■7001 ▼aZhao, L.
■7001 ▼aQi, H.
■7001 ▼aLi, F.
■7001 ▼aXue, J.
■773 ▼tBone=International Bone and Mineral Society▼gVol. 42 No. 4 (2008. 4)▼d2008, 04
■856 ▼uhttp://www.elsevier.com/locate/bone
■SIS ▼aS047480▼b60077318▼h8▼s2▼fP
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