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High throughput screening of human subtelomeric DNA for copy number changes using multiplex amplifiable probe hybridisation (MAPH)

Background: Subtelomeric regions of the human genome are gene rich, with a high level of sequence polymorphism. A number of clinical conditions, including learning disability, have been attributed to subtelomeric deletions or duplications, but screening for deletion in these regions using convention...

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Bibliografiske detaljer
Main Authors: Hollox, E, Atia, T, Cross, G, Parkin, T, Armour, J
Format: Artigo
Sprog:Inglês
Udgivet: BMJ Group 2002
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735019/
https://ncbi.nlm.nih.gov/pubmed/12414816
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.39.11.790
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