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Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long arm.
Cytogenetic re-evaluation of a fibroblast cell line from a female Hunter's syndrome case with a balanced X;autosome translocation, which had previously been reported to have a breakpoint in Xq26 to Xq27, showed the breakpoint to be either between Xq27 and Xq28 or within Xq28. The normal X chrom...
Tallennettuna:
| Julkaisussa: | J Med Genet |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMJ Publishing Group
1989
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015597/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2499679/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.26.5.309 |
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