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Annals of Human Genetics|May 1, 1991
Genetic linkage between the Kell blood group system and prolactin-inducible protein loci: provisional assignment of KEL to chromosome 7T Zelinski, G Coghlan, Y Myal, et al.
Human Genetics|October 1, 1993
Identification of an uncommon haptoglobin type using DNA and protein analysisS L Marles, P J McAlpine, T Zelinski, et al.
Vox Sanguinis|January 1, 1988
The Swann phenotype 700:4,-41; genetic studiesM Lewis, H Kaita, S Philipps, et al.
British Journal of Haematology|May 1, 1996
Molecular analysis of blood group Rh transcripts from a rGr variantI Mouro, Y Colin, P Gane, et al.
Transfusion|September 1, 1988
The Colton blood group locus. A linkage analysisT Zelinski, H Kaita, M Lewis, et al.
American Journal of Human Genetics|June 23, 1998
A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locusT Weiler, C R Greenberg, T Zelinski, et al.
Blood Cells, Molecules & Diseases|September 28, 2011
Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindredB L Houston, T Zelinski, S J Israels, et al.
American Journal of Human Genetics|July 1, 1992
Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type IA Wiens, S Marles, J Safneck, et al.
American Journal of Medical Genetics|October 23, 1997
Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD lociT Weiler, C R Greenberg, E Nylen, et al.
Vox Sanguinis|December 31, 2013
International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Cancun report (2012)J R Storry, L Castilho, G Daniels, et al.
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