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Image Search Results
Journal: Birth Defects Research. Part A, Clinical and Molecular Teratology
Article Title: De Novo Deletion of Chromosome 20q13.33 in a Patient with Tracheo-esophageal Fistula, Cardiac Defects and Genitourinary Anomalies Implicates GTPBP5 as a Candidate Gene
doi: 10.1002/bdra.20821
Figure Lengend Snippet: De novo 0.7 Mb deletion of chromosome 20q13.33 in the patient described here, ascertained with Illumina Omni1-Quad high-density single-nucleotide polymorphism (SNP) microarray platform, and visualized using GenomeStudio (v2009.2, www.Illumina.com ) genotyping module. The deletion is indicated by the arrow ; the corresponding chromosomal region is outlined in the ideogram below. The proband's microarray is uppermost; parental arrays of the same region are shown below the proband's. [Color figure can be viewed in the online issue, which is available at wileyonlinelibrary.com .]
Article Snippet: This deletion was confirmed by
Techniques: Microarray