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Arthroscopy : the Journal of Arthroscopic & Related Surgery : Official Publication of the Arthroscopy Association of North America and the International Arthroscopy Association|October 16, 2004
Spontaneous rupture of the popliteus tendon in a 74-year-old woman and review of the literatureJames R D Murray, Julian R B Grundy, Iona E Collins, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1993
A Gla domain mutation (Arg 15-->Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosisD S Millar, C B Grundy, P Bignell, et al.
Human Genetics|March 1, 1993
A novel nonsense mutation in the protein C (PROC) gene (Trp-29-->term) causing recurrent venous thrombosisD S Millar, C B Grundy, P Bignell, et al.
Blood|August 15, 1991
Recurrent deletion in the human antithrombin III geneC B Grundy, F Thomas, D S Millar, et al.
Human Genetics|August 1, 1990
Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locusP Jedlicka, S Greer, D S Millar, et al.
Journal of Integrative Plant Biology|March 24, 2025
Functional genomics dissection of the nodulation autoregulation pathway (AON) in soybean (Glycine max)Peter M Gresshoff, Chao Su, Huanan Su, et al.
Genomics|August 1, 1992
De novo splice site mutation in the antithrombin III (AT3) gene causing recurrent venous thrombosis: demonstration of exon skipping by ectopic transcript analysisL P Berg, C B Grundy, F Thomas, et al.
Human Genetics|December 1, 1990
The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII geneD S Millar, R A Steinbrecher, K Wieland, et al.
Sexually Transmitted Infections|July 21, 2006
Screening for Chlamydia trachomatis in asymptomatic women attending outpatient clinics in a large maternity hospital in Dublin, IrelandH M McMillan, H O'Carroll, J S Lambert, et al.
Blood|December 1, 1990
The molecular genetic analysis of hemophilia A: a directed search strategy for the detection of point mutations in the human factor VIII geneJ K Pattinson, D S Millar, J H McVey, et al.
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