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Volumn 52, Issue 1, 1997, Pages 12-16

Incomplete penetrance and expressivity skewing in hereditary multiple exostoses

Author keywords

Chondrosarcoma; Incomplete penetrance; Multiple exostoses

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BONE DISEASE; CANCER RISK; CHONDROSARCOMA; CONTROLLED STUDY; DEGENERATION; FAMILY HISTORY; FEMALE; HEREDITARY MULTIPLE EXOSTOSIS; HUMAN; HUMAN CELL; LONG BONE; MAJOR CLINICAL STUDY; MALE; ONSET AGE; PEDIGREE ANALYSIS; PENETRANCE; PRIORITY JOURNAL; SEX DIFFERENCE;

EID: 0030829353     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1997.tb02508.x     Document Type: Article
Times cited : (125)

References (13)
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    • Canella, P.1    Gardini, F.2    Boriani, S.3
  • 4
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    • Hereditary multiple exostoses
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    • Hennekam, R.M.C.1
  • 5
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    • Hereditary multiple exostosis
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    • (1943) Arch Pathol , vol.36 , pp. 335-357
    • Jaffe, H.L.1
  • 8
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    • (1959) Am J Hum Genet , vol.11 , pp. 1-16
    • Morton, N.1
  • 10
    • 0001524698 scopus 로고
    • Hereditary multiple exostosis
    • Solomon L. Hereditary multiple exostosis. Am J Hum Genet 1964: 16: 351-363.
    • (1964) Am J Hum Genet , vol.16 , pp. 351-363
    • Solomon, L.1
  • 11
    • 0020545180 scopus 로고
    • The infrequency of malignant disease in diaphyseal aclasis and neurofibromatosis
    • Voutsinas S, Wynne-Davis R The infrequency of malignant disease in diaphyseal aclasis and neurofibromatosis. J Med Genet 1983: 20: 345-349.
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    • Voutsinas, S.1    Wynne-Davis, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.