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Prenatal Diagnosis
|
November 1, 1985
Normal blood cell values in the early mid-trimester fetus
D S Millar, L R Davis, C H Rodeck, et al.
Analytical Biochemistry
|
April 10, 1995
Solid-phase hybridization capture of low-abundance target DNA sequences: application to the polymerase chain reaction detection of Mycobacterium paratuberculosis and Mycobacterium avium subsp. silvaticum
D S Millar, S J Withey, M L Tizard, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
April 1, 1995
Three novel mutations in the protein C (PROC) gene causing venous thrombosis
D S Millar, D Bevan, A Chitolie, et al.
Human Genetics
|
January 1, 1991
Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicism
K Wieland, D S Millar, C B Grundy, et al.
Blood
|
September 15, 1996
Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasma
P Simioni, M Kalafatis, D S Millar, et al.
Nucleic Acids Research
|
October 23, 1997
Detection and measurement of PCR bias in quantitative methylation analysis of bisulphite-treated DNA
P M Warnecke, C Stirzaker, J R Melki, et al.
Oncogene
|
February 18, 1999
Detailed methylation analysis of the glutathione S-transferase pi (GSTP1) gene in prostate cancer
D S Millar, K K Ow, C L Paul, 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 thrombosis
D S Millar, C B Grundy, P Bignell, et al.
British Journal of Haematology
|
November 1, 1993
A novel dysfunctional protein C (protein C Padua 2) associated with a thrombotic tendency: substitution of Cys for Arg-1 results in a strongly reduced affinity for binding of Ca++
A Girolami, P Simioni, B Girolami, et al.
Human Genetics
|
October 1, 1990
Detection of a novel point mutation causing haemophilia A by PCR/direct sequencing of ectopically-transcribed factor VIII mRNA
L P Berg, K Wieland, D S Millar, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
Prenatal Diagnosis
|
November 1, 1985
Normal blood cell values in the early mid-trimester fetus
D S Millar, L R Davis, C H Rodeck, et al.
Analytical Biochemistry
|
April 10, 1995
Solid-phase hybridization capture of low-abundance target DNA sequences: application to the polymerase chain reaction detection of Mycobacterium paratuberculosis and Mycobacterium avium subsp. silvaticum
D S Millar, S J Withey, M L Tizard, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
April 1, 1995
Three novel mutations in the protein C (PROC) gene causing venous thrombosis
D S Millar, D Bevan, A Chitolie, et al.
Human Genetics
|
January 1, 1991
Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicism
K Wieland, D S Millar, C B Grundy, et al.
Blood
|
September 15, 1996
Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasma
P Simioni, M Kalafatis, D S Millar, et al.
Nucleic Acids Research
|
October 23, 1997
Detection and measurement of PCR bias in quantitative methylation analysis of bisulphite-treated DNA
P M Warnecke, C Stirzaker, J R Melki, et al.
Oncogene
|
February 18, 1999
Detailed methylation analysis of the glutathione S-transferase pi (GSTP1) gene in prostate cancer
D S Millar, K K Ow, C L Paul, 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 thrombosis
D S Millar, C B Grundy, P Bignell, et al.
British Journal of Haematology
|
November 1, 1993
A novel dysfunctional protein C (protein C Padua 2) associated with a thrombotic tendency: substitution of Cys for Arg-1 results in a strongly reduced affinity for binding of Ca++
A Girolami, P Simioni, B Girolami, et al.
Human Genetics
|
October 1, 1990
Detection of a novel point mutation causing haemophilia A by PCR/direct sequencing of ectopically-transcribed factor VIII mRNA
L P Berg, K Wieland, D S Millar, et al.
Page
of 4