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Volumn 16, Issue 1, 2006, Pages 69-

Noonan syndrome with giant cell lesions

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 12; CHROMOSOME 4; DIFFERENTIAL DIAGNOSIS; FIBROUS DYSPLASIA; GENETICS; HUMAN; MANDIBLE TUMOR; MUTATION; NOONAN SYNDROME; NOTE; OSTEOCLASTOMA;

EID: 33644967569     PISSN: 09607439     EISSN: 1365263X     Source Type: Journal    
DOI: 10.1111/j.1365-263X.2006.00728.x     Document Type: Letter
Times cited : (1)

References (10)
  • 4
    • 0034977079 scopus 로고    scopus 로고
    • Mutations in the gene encoding c-Abl-binding protein SH3BP2 cause cherubism
    • Ueki Y Tiziani V Santanna C et al. Mutations in the gene encoding c-Abl-binding protein SH3BP2 cause cherubism Nature Genetics 2001 28 125 126
    • (2001) Nature Genetics , vol.28 , pp. 125-126
    • Ueki, Y.1    Tiziani, V.2    Santanna, C.3
  • 5
    • 18344385476 scopus 로고    scopus 로고
    • Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
    • Tartaglia M Mehler EL Goldberg R et al. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome Nature Genetics 2001 29 465 468
    • (2001) Nature Genetics , vol.29 , pp. 465-468
    • Tartaglia, M.1    Mehler, E.L.2    Goldberg, R.3
  • 6
  • 7
    • 18844428291 scopus 로고    scopus 로고
    • Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndrome
    • Lee JS Tartagla M Gelb BD et al. Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndrome Journal of Medical Genetics 2005 42 e11
    • (2005) Journal of Medical Genetics , vol.42 , pp. 11
    • Lee, J.S.1    Tartagla, M.2    Gelb, B.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.