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A Chinese familial growth hormone deficiency with a deletion of 7.1 kb of DNA.
Using restriction endonuclease analysis and a human growth hormone cDNA probe, we have found a Chinese family with a human growth hormone gene deletion. Two affected sibs are homozygous for a deletion of approximately 7.1 kb of DNA, which contains the normal human growth hormone gene. The patients&#...
Guardat en:
| Publicat a: | J Med Genet |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Publishing Group
1990
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016995/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2325087/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.27.3.151 |
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