Molecular karyotyping in patients with mental retardation using 100K single‐nucleotide polymorphism arrays

BACKGROUND: Using array techniques, it was recently shown that about 10% of patients with mental retardation of unknown origin harbour cryptic chromosomal aneusomies. However, data analysis is currently not standardised and little is known about its sensitivity and specificity. METHODS: We have deve...

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Bibliografiske detaljer
Main Authors: Hoyer, Juliane, Dreweke, Alexander, Becker, Christian, Göhring, Ina, Thiel, Christian T, Peippo, Maarit M, Rauch, Ralf, Hofbeck, Michael, Trautmann, Udo, Zweier, Christiane, Zenker, Martin, Hüffmeier, Ulrike, Kraus, Cornelia, Ekici, Arif B, Rüschendorf, Franz, Nürnberg, Peter, Reis, André, Rauch, Anita
Format: Artigo
Sprog:Inglês
Udgivet: BMJ Group 2007
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Original Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2597959/
https://ncbi.nlm.nih.gov/pubmed/17601928
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2007.050914
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