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The use of restriction fragment length polymorphisms in prenatal diagnosis of dihydropteridine reductase deficiency.

Using a human dihydropteridine reductase (hDHPR) cDNA probe we have detected two AvaII and one MspI restriction fragment length polymorphisms (RFLPs). We show that these RFLPs are in disequilibrium and calculate that approximately 60% of Caucasians are heterozygous for at least one RFLP. We demonstr...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Dahl, H H, Wake, S, Cotton, R G, Danks, D M
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1988
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1015417/
https://ncbi.nlm.nih.gov/pubmed/2895188
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