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  • Ljung, R.C.R. (author)
  • Prenatal diagnosis of haemophilia
  • 1999
  • In: Haemophilia. - : Wiley. - 1351-8216 .- 1365-2516. ; 5:2, s. 84-87
  • Research review (peer-reviewed)abstract
    • Genotype assessment based on direct identification of the pathogenic mutation in a chorionic villi sample obtained in the 11-12th gestational week is the most reliable method for prenatal diagnosis and should be used if available. Genetic linkage studies of polymorphisms should be the second choice in the assessment of carriers and in prenatal diagnosis. Carriers of haemophilia should be offered adequate psychosocial support before, during and after the prenatal diagnostic procedures.
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Type of publication
research review (1)
Type of content
peer-reviewed (1)
Author/Editor
Ljung, R. C.R. (1)
University
Lund University (1)
Language
English (1)
Research subject (UKÄ/SCB)
Medical and Health Sciences (1)
Year

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