Osteoglophonic dysplasia: A ‘common’ mutation in a rare disease

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dc.contributor.authorSow, AJ
dc.contributor.authorRamli, R.
dc.contributor.authorLatiff, ZA
dc.contributor.authorIchikawa, S.
dc.contributor.authorGray, AK
dc.contributor.authorNordin, R.
dc.contributor.authorAbd Jabar, MN
dc.contributor.authorPrimuharsa Putra, SHA
dc.contributor.authorSiar, CH
dc.contributor.authorEcons, MJ
dc.contributor.departmentDepartment of Medicine, IU School of Medicineen_US
dc.date.accessioned2015-11-02T21:14:50Z
dc.date.available2015-11-02T21:14:50Z
dc.date.issued2010-08
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationSow, A., Ramli, R., Latiff, Z., Ichikawa, S., Gray, A., Nordin, R., … Econs, M. (2010). Osteoglophonic dysplasia: A “common” mutation in a rare disease. Clinical Genetics, 78(2), 197–198. http://doi.org/10.1111/j.1399-0004.2010.01382.xen_US
dc.identifier.urihttps://hdl.handle.net/1805/7316
dc.language.isoen_USen_US
dc.publisherWiley Online Libraryen_US
dc.relation.isversionof10.1111/j.1399-0004.2010.01382.xen_US
dc.relation.journalClinical Geneticsen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectdwarfismen_US
dc.subjectmutationsen_US
dc.subjectdysplasiaen_US
dc.subjectfibroblasten_US
dc.subjectgrowth factoren_US
dc.subjectreceptoren_US
dc.subjectinheriteden_US
dc.subjectcraniofacialen_US
dc.subjectprognathismen_US
dc.subjecthypertelorismen_US
dc.subjecthypertrophicen_US
dc.subjecthypoplasiaen_US
dc.subjectcraniosynostosisen_US
dc.titleOsteoglophonic dysplasia: A ‘common’ mutation in a rare diseaseen_US
dc.typeArticleen_US
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