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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...
Gardado en:
| Publicado en: | J Med Genet |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BMJ Publishing Group
1989
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015530/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2783976/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.26.1.10 |
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