Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfecta.

One cloned complementary DNA and one genomic subclone were used to detect restriction fragment length polymorphism associated with the pro alpha 2(I) gene for human type I procollagen. The restriction fragments obtained from examination of 30-122 chromosomes confirmed previous indications that the p...

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Pubblicato in:	J Clin Invest
Autori principali:	Tsipouras, P, Myers, J C, Ramirez, F, Prockop, D J
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	American Society for Clinical Investigation 1983
Soggetti:	Research Article
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC370410/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6313757/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI111082
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