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21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.

During our investigations of polymorphisms at, and in the immediate chromosomal vicinity of, the 21-hydroxylase locus in families with 21-hydroxylase deficiency, three families were found to show marked discordance in clinical features of HLA identical subjects. In one family, there is discordance b...

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Bibliografski detalji
Glavni autori: Sinnott, P J, Dyer, P A, Price, D A, Harris, R, Strachan, T
Format: Artigo
Jezik:Inglês
Izdano: 1989
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1015530/
https://ncbi.nlm.nih.gov/pubmed/2783976
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