Cosegregation of hypertrophic cardiomyopathy and a fragile site on chromosome 16 in a large Italian family.
We studied the karyotypes of 10 members of a family in whom hypertrophic cardiomyopathy is segregating as an autosomal dominant trait. In all those affected by the disease, a fragile site on the long arm of chromosome 16 was found, expressed with different frequencies, but the unaffected family memb...
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| Publicado no: | J Med Genet |
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| Principais autores: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
1990
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1017132/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2359098/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.27.6.363 |
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