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Journal of Medical Genetics|December 1, 1992
Severity of chest disease in cystic fibrosis patients in relation to their genotypesL N al-Jader, A L Meredith, H C Ryley, et al.Journal of Medical Genetics|December 1, 1992
Predicted and observed sizes of dystrophin in some patients with gene deletions that disrupt the open reading frameL V Nicholson, K M Bushby, M A Johnson, et al.Journal of Medical Genetics|March 1, 1992
Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probesJ Melki, S Abdelhak, P Burlet, et al.Journal of Medical Genetics|September 1, 1992
Mutation analysis of 184 cystic fibrosis families in WalesJ Cheadle, J Myring, L al-Jader, et al.Journal of Medical Genetics|July 1, 1992
The aggregation of the 5' insulin gene polymorphism in insulin dependent (type I) diabetes mellitus familiesL J Raffel, G A Hitman, H Toyoda, et al.Journal of Medical Genetics|July 1, 1992
Site specific screening for point mutations in ornithine transcarbamylase deficiencyD Feldmann, J M Rozet, A Pelet, et al.Journal of Medical Genetics|July 1, 1992
Genetic variation at fibrinogen loci and plasma fibrinogen levelsJ M Connor, F G Fowkes, J Wood, et al.Journal of Medical Genetics|January 20, 2004
The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loadingK J Livesey, V L C Wimhurst, K Carter, et al.Journal of Medical Genetics|December 20, 2003
Somatic instability of the DNA sequences encoding the polymorphic polyglutamine tract of the AIB1 geneP Dai, L-J C WongJournal of Medical Genetics|February 1, 1978
Down syndrome and recent demographic trends in ManitobaJ A Evans, A G Hunter, J L HamertonPageof 649