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  • Ljung, R.C.R.Lund University,Lunds universitet,Pediatrik, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Paediatrics (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine,Skåne University Hospital (author)

Prenatal diagnosis of haemophilia

  • Article/chapterEnglish1999

Publisher, publication year, extent ...

  • 2002-04-25
  • Wiley,1999
  • 4 s.

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  • LIBRIS-ID:oai:lup.lub.lu.se:6c85d421-172b-4c87-ae1e-9d6fcfee9e89
  • https://lup.lub.lu.se/record/6c85d421-172b-4c87-ae1e-9d6fcfee9e89URI
  • https://doi.org/10.1046/j.1365-2516.1999.00295.xDOI

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  • Language:English
  • Summary in:English

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Notes

  • 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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  • Pediatrik, LundSektion V (creator_code:org_t)

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  • In:Haemophilia: Wiley5:2, s. 84-871351-82161365-2516

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By the author/editor
Ljung, R.C.R.
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Clinical Medicin ...
and Hematology
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Clinical Medicin ...
and Pediatrics
Articles in the publication
Haemophilia
By the university
Lund University

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