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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/19331
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dc.contributor.authorSuthers, Graeme Kembleen
dc.date.issued1990en
dc.identifier.urihttp://hdl.handle.net/2440/19331-
dc.descriptionTypescript (Photocopy)en
dc.descriptionIncludes published papers co-authored by the author at the end of volume 2en
dc.descriptionBibliography: leaves 195-237 of vol. 1en
dc.description2 v. : ill ; 30 cm.en
dc.format.extent53471 bytesen
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.subject.ddc616.85/88042 20en
dc.subject.lcshFragile X syndrome.en
dc.subject.lcshHuman chromosome abnormalities.en
dc.subject.lcshLinkage (Genetics)en
dc.subject.lcshMental retardation Genetic aspects.en
dc.titleThe human gene map near the fragile X / by Graeme Kemble Suthersen
dc.typeThesisen
dc.contributor.schoolDept. of Paediatrics, Faculty of Medicineen
dc.provenanceCopyright material removed from digital thesis. See print copy in University of Adelaide Library for full text. This electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exception. If you are the author of this thesis and do not wish it to be made publicly available or If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals-
dc.description.dissertationThesis (Ph.D.)--Dept. of Paediatrics, Faculty of Medicine, University of Adelaide, 1991en
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