6p.24 microdeletion involving TFAP2A without classic features of branchio-oculo-facial syndrome

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dc.contributor.authorLeblanc, S.K.
dc.contributor.authorYu, S.
dc.contributor.authorBarnett, C.P.
dc.date.issued2013
dc.descriptionLetter to the Editor
dc.description.statementofresponsibilityShannon K. LeBlanc, Sui Yu, and Christopher P. Barnett
dc.identifier.citationAmerican Journal of Medical Genetics, Part A, 2013; 161(4):901-904
dc.identifier.doi10.1002/ajmg.a.35804
dc.identifier.issn1552-4825
dc.identifier.issn1552-4833
dc.identifier.orcidBarnett, C.P. [0000-0003-1717-3824]
dc.identifier.urihttp://hdl.handle.net/2440/95579
dc.language.isoen
dc.publisherWiley
dc.rightsCopyright © 2013 Wiley Periodicals, Inc.
dc.source.urihttps://doi.org/10.1002/ajmg.a.35804
dc.subjectBranchio-Oto-Renal Syndrome
dc.title6p.24 microdeletion involving TFAP2A without classic features of branchio-oculo-facial syndrome
dc.typeJournal article
pubs.publication-statusPublished

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