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Prenatal diagnosis ...
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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 ...
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2002-04-25
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Wiley,1999
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4 s.
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LIBRIS-ID:oai:lup.lub.lu.se:6c85d421-172b-4c87-ae1e-9d6fcfee9e89
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https://lup.lub.lu.se/record/6c85d421-172b-4c87-ae1e-9d6fcfee9e89URI
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https://doi.org/10.1046/j.1365-2516.1999.00295.xDOI
Supplementary language notes
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Language:English
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Summary in:English
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Subject category:for swepub-publicationtype
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Subject category:ref swepub-contenttype
Notes
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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)
Related titles
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In:Haemophilia: Wiley5:2, s. 84-871351-82161365-2516
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