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Carrier detection in xeroderma pigmentosum.

We were able to detect clinically normal carriers of xeroderma pigmentosum (XP) genes with coded samples of either peripheral blood lymphocytes or skin fibroblasts, using a cytogenetic assay shown previously to detect individuals with cancer-prone genetic disorders. Metaphase cells of phytohemagglut...

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Detalles Bibliográficos
Publicado en:J Clin Invest
Principais autores: Parshad, R, Sanford, K K, Kraemer, K H, Jones, G M, Tarone, R E
Formato: Artigo
Idioma:Inglês
Publicado: American Society for Clinical Investigation 1990
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Acceso en liña:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC296397/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2295692/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI114403
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