ArticleBirth defects research. Part A, Clinical and molecular teratology2011
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.
Benjamin D Solomon et al.PubMed ↗Full text ↗Publisher ↗
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