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dc.contributor.authorCraig, Jamie E
dc.contributor.authorSale, Michele M
dc.contributor.authorMackey, David A
dc.contributor.authorRussell-Eggit, Isabelle M
dc.contributor.authorWirth, M Gabriela
dc.contributor.authorDickinson, Joanne L
dc.contributor.authorElder, James E
dc.contributor.authorBurdon, Kathryn Penelope
dc.date.accessioned2010-07-27T05:52:53Z
dc.date.available2010-07-27T05:52:53Z
dc.date.issued2004en_US
dc.identifier.citationBurdon, K.P., Wirth, M., Mackey, D.A., Russell-Eggit, I M, Craig, J., Elder, J.E., Dickinson, J.L., & Sale, M.M., 2004. A novel mutation in the Connexin 46 Gene causes autosomal dominant congenital cataract with incomplete penetrance. Journal of Medical Genetics, 41(8).en
dc.identifier.issn0022-2593en_US
dc.identifier.urihttp://hdl.handle.net/2328/9260
dc.titleA novel mutation in the Connexin 46 Gene causes autosomal dominant congenital cataract with incomplete penetranceen_US
dc.typeArticleen_US
dc.identifier.rmid2004054737en_US
dc.identifier.doihttps://doi.org/10.1136/jmg.2004.018333en
dc.description.noteBRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON, ENGLAND, WC1H 9JRen
dc.subject.forgroup0604 Geneticsen_US
dc.subject.forgroup1103 Clinical Sciencesen_US


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  • 0604 - Genetics
    Flinders' staff research in Genetics, reportable as part of ERA, 2001-

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