Chromosomal copy number changes in patients with non‐syndromic X linked mental retardation detected by array CGH

Several studies have shown that array based comparative genomic hybridisation (CGH) is a powerful tool for the detection of copy number changes in the genome of individuals with a congenital disorder. In this study, 40 patients with non‐specific X linked mental retardation were analysed with full co...

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Bibliografiset tiedot
Päätekijät: Lugtenberg, D, de Brouwer, A P M, Kleefstra, T, Oudakker, A R, Frints, S G M, Schrander‐Stumpel, C T R M, Fryns, J P, Jensen, L R, Chelly, J, Moraine, C, Turner, G, Veltman, J A, Hamel, B C J, de Vries, B B A, van Bokhoven, H, Yntema, H G
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BMJ Group 2006
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Original Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2563232/
https://ncbi.nlm.nih.gov/pubmed/16169931
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.036178
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