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Elevated sister chromatid exchange phenotype of Bloom syndrome cells is complemented by human chromosome 15.

Bloom syndrome (BSx) is a rare autosomal-recessive chromosome-instability disorder manifested by a constellation of clinical features including a significant predisposition to early onset of neoplasia. BSx cells display cytogenetic abnormalities, the pathognomonic feature being an increased rate of...

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Detalles Bibliográficos
Autores principales: McDaniel, L D, Schultz, R A
Formato: Artigo
Lenguaje:Inglês
Publicado: 1992
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC49836/
https://ncbi.nlm.nih.gov/pubmed/1518822
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