High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results

BACKGROUND: Diagnostic analysis of patients with developmental disorders has improved over recent years largely due to the use of microarray technology. Array methods that facilitate copy number analysis have enabled the diagnosis of up to 20% more patients with previously normal karyotyping results...

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Hoofdauteurs: Siggberg, Linda, Sirpa, Ala-Mello, Tarja, Linnankivi, Kristiina, Avela, Ilari, Scheinin, Kati, Kristiansson, Päivi, Lahermo, Marja, Hietala, Liisa, Metsähonkala, Esa, Kuusinen, Maarit, Laaksonen, Janna, Saarela, Sakari, Knuutila
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2012
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3523000/
https://ncbi.nlm.nih.gov/pubmed/22984989
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-13-84
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