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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/2921
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dc.contributor.authorGraham, J. M.en
dc.contributor.authorWheeler, P.en
dc.contributor.authorTackels-Horne, Darcien
dc.contributor.authorLin, Angela E.en
dc.contributor.authorHall, Bryan D.en
dc.contributor.authorMay, Melanieen
dc.contributor.authorShort, K. M.en
dc.contributor.authorSchwartz, Charles E.en
dc.contributor.authorCox, T. C.en
dc.date.issued2003en
dc.identifier.citationAmerican Journal of Medical Genetics. Part A, 2003; 123A(1):37-44en
dc.identifier.issn1552-4825en
dc.identifier.issn1552-4833-
dc.identifier.urihttp://hdl.handle.net/2440/2921-
dc.descriptionThe definitive version may be found at www.wiley.comen
dc.description.statementofresponsibilityJohn M. Graham Jr, Patricia Wheeler, Darci Tackels-Horne, Angela E. Lin, Bryan D. Hall, Melanie May, Kieran M. Short, Charles E. Schwartz, Timothy C. Coxen
dc.language.isoenen
dc.publisherWiley-Lissen
dc.rights© 2003 Wiley-Liss, Inc.-
dc.source.urihttp://www3.interscience.wiley.com/journal/104556616/abstracten
dc.titleA new X-linked syndrome with agenesis of the corpus callosum, mental retardation, coloboma, micrognathia, and a mutation in the Alpha 4 gene at Xq13en
dc.typeJournal articleen
dc.contributor.organisationCentre for the Molecular Genetics of Developmenten
dc.identifier.doi10.1002/ajmg.a.20504en
Appears in Collections:Centre for the Molecular Genetics of Development publications
Molecular and Biomedical Science publications

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