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Gamma thalassemia resulting from the deletion of a gamma-globin gene.
The first example of a deletion of one of the two gamma globin genes has been characterized through an analysis of the DNA of the heterozygous parent of a homozygous newborn, using restriction endonuclease mapping techniques. A deletion of approximately 5 kb was observed which was probably caused by...
Bewaard in:
| Hoofdauteurs: | , , , , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
1983
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| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC326070/ https://ncbi.nlm.nih.gov/pubmed/6306596 |
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