A familial deletion of 16q21 characterized by an SNP array and associated with a normal phenotype

2013

Additional Metadata
Persistent URL	doi.org/10.1002/ajmg.a.35912, hdl.handle.net/1765/53746
Journal	American Journal of Medical Genetics. Part A
Organisation	Erasmus MC: University Medical Center Rotterdam
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	Kowalczyk, M., Tomaszewska, R., Podbiol-Palenta, A., Remiszewska, B., Galjaard, R.-J., Zajaczek, S., & Srebniak, M. (2013). A familial deletion of 16q21 characterized by an SNP array and associated with a normal phenotype. American Journal of Medical Genetics. Part A, 161(6), 1501–1504. doi:10.1002/ajmg.a.35912

Publication