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Volumn 12, Issue 7, 1992, Pages 575-586

Five years' experience of prenatal diagnosis of cystic fibrosis in the former U.S.S.R.

Author keywords

CFTR gene mutations; Cystic fibrosis; Microvillar enzymes; Prenatal diagnosis; RFLP

Indexed keywords

ARTICLE; CYSTIC FIBROSIS; DIAGNOSTIC ACCURACY; DNA DETERMINATION; ETHNIC GROUP; FAMILY STUDY; FETUS; GENE MUTATION; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; PRENATAL DIAGNOSIS; USSR;

EID: 0026647397     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1970120703     Document Type: Article
Times cited : (16)

References (22)
  • 4
    • 0021978460 scopus 로고
    • A comparative study of microvillar enzyme activities in the prenatal diagnosis of cystic fibrosis
    • (1985) Prenat. Diagn. , vol.5 , pp. 129-134
    • Brock, D.J.H.1
  • 15
    • 84995086898 scopus 로고
    • The progress and outcome of cystic fibrosis in children after modern treatment and rehabilitation, Doctor's Thesis Abstracts, Moscow
    • (1986) , pp. 44
    • Kapranov, N.I.1
  • 17
    • 84995107772 scopus 로고
    • Abnormal frequency of delF508 mutation in neonatal transitory hypertrypsinemia
    • (1991) Lancet , vol.337 , pp. 73
    • Laroche, D.1    Travert, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.