Parental origin of chromosome 15 deletion in Prader-Willi syndrome

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dc.contributor.authorButler, Merlin G.
dc.contributor.authorPalmer, Catherine G.
dc.contributor.departmentMedical and Molecular Genetics, School of Medicineen_US
dc.date.accessioned2018-05-15T18:09:30Z
dc.date.available2018-05-15T18:09:30Z
dc.date.issued1983-06-04
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationButler, M. G., & Palmer, C. G. (1983). PARENTAL ORIGIN OF CHROMOSOME 15 DELETION IN PRADER-WILLI SYNDROME. Lancet (London, England), 1(8336), 1285–1286.en_US
dc.identifier.urihttps://hdl.handle.net/1805/16186
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.journalLanceten_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectChromosome deletionen_US
dc.subjectChromosomes, Human, 13-15en_US
dc.subjectPrader-Willi syndromeen_US
dc.titleParental origin of chromosome 15 deletion in Prader-Willi syndromeen_US
dc.typeArticleen_US
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