Genome-Wide Oligonucleotide Array Comparative Genomic Hybridization for Etiological Diagnosis of Mental Retardation: A Multicenter Experience of 1499 Clinical Cases

To assess the clinical utility of genome-wide oligonucleotide arrays in diagnosis of mental retardation and to address issues relating to interpretation of copy number changes (CNCs), we collected results on a total of 1499 proband patients from five academic diagnostic laboratories where the same 4...

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Bibliografiset tiedot
Päätekijät: Xiang, Bixia, Zhu, Hongbo, Shen, Yiping, Miller, David T., Lu, Kangmo, Hu, Xiaofeng, Andersson, Hans C., Narumanchi, Tarachandra M., Wang, Yueying, Martinez, Jose E., Wu, Bai-Lin, Li, Peining, Li, Marilyn M., Chen, Tian-Jian, Fan, Yao-Shan
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Society for Investigative Pathology 2010
Aiheet:
Regular Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2871727/
https://ncbi.nlm.nih.gov/pubmed/20093387
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/jmoldx.2010.090115
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