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Article

2.3 Mb terminal deletion in 12p13.33 associated with oculoauriculovertebral spectrum and evaluation of WNT5B as a candidate gene

4 Sept 2009

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Share to Congenital Ear and Nasal Anomalies
Share to Genomic variations and chromosomal abnormalities
Share to Wnt/β-catenin signaling in development and cancer

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 19733267
DOI: 10.1016/j.ejmg.2009.08.005

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