Phenotypic Variability Associated with a Large Recurrent 1q21.1 Microduplication in a Three-Generation Family

2015

Molecular Syndromology , Volume 6 - Issue 2 p. 71- 76

Additional Metadata
Keywords	1q21.1 microduplication, Congenital heart defects, Copy number variation, GJA5
Persistent URL	doi.org/10.1159/000431274, hdl.handle.net/1765/81657
Journal	Molecular Syndromology
Organisation	Department of Clinical Genetics
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Verhagen, J.M.A, de Leeuw, N, Papatsonis, D.N.M, Grijseels, E.W.M, de Krijger, R.R, & Wessels, M.W. (2015). Phenotypic Variability Associated with a Large Recurrent 1q21.1 Microduplication in a Three-Generation Family. Molecular Syndromology, 6(2), 71–76. doi:10.1159/000431274

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