Human Genome Epidemiology Literature Finder
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Query Trace: WDR63[original query] |
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Targeted copy number screening highlights an intragenic deletion of WDR63 as the likely cause of human occipital encephalocele and abnormal CNS development in zebrafish. Human mutation 2017 12 39 (4): 495-505. Hofmeister Wolfgang, Pettersson Maria, Kurtoglu Deniz, Armenio Miriam, Eisfeldt Jesper, Papadogiannakis Nikos, Gustavsson Peter, Lindstrand An |
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- Page last updated:Apr 29, 2024
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