D P Lillicrap - JoVE Visualize

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British Journal of Haematology|June 1, 1990

A mutation adjacent to the beta cleavage site of factor IX (valine 182 to leucine) results in mild haemophilia BmS A Taylor, M B Liddell, I R Peake, et al.

British Journal of Haematology|March 1, 1986

Comparison of phenotypic assessment and the use of two restriction fragment length polymorphisms in the diagnosis of the carrier state in haemophilia BD P Lillicrap, M B Liddell, R J Matthews, et al.

Blood|April 1, 1991

Cosegregation of von Willebrand factor gene polymorphisms and possible germinal mosaicism in type IIB von Willebrand diseaseE W Murray, A R Giles, P J Bridge, et al.

Human Genetics|July 1, 1988

A complete deletion of the factor IX gene and new TaqI variant in a hemophilia B kindredS A Taylor, D P Lillicrap, V Blanchette, et al.

American Journal of Human Genetics|August 1, 1990

Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human geneD D Koeberl, C D Bottema, R P Ketterling, et al.

British Journal of Haematology|August 1, 1989

Factor IX Cardiff: a variant factor IX protein that shows abnormal activation is caused by an arginine to cysteine substitution at position 145M B Liddell, I R Peake, S A Taylor, et al.

American Journal of Clinical Pathology|October 1, 1989

Absence of a bleeding tendency in severe acquired von Willebrand's disease. The role of platelet von Willebrand factor in maintaining normal hemostasisJ Drouin, D P Lillicrap, C A Izaguirre, et al.

Retina (Philadelphia, Pa.)|April 26, 2001

Prevalence of factor V Leiden and activated protein C resistance in central retinal vein occlusionT M Johnson, S El-Defrawy, W G Hodge, et al.

Blood|January 1, 1990

Variation of the non-factor VIII sequences detected by a probe from intron 22 of the factor VIII geneD P Lillicrap, S A Taylor, P C Schuringa, et al.

American Journal of Medical Genetics|March 1, 1987

Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere-fra(X)-DXS15-DXS52-F8C-telomereL M Mulligan, H J Grover, V S Blanchette, et al.

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Showing results (21-30 of 33) with videos related to

Sort By:

Pageof 4

British Journal of Haematology|June 1, 1990

A mutation adjacent to the beta cleavage site of factor IX (valine 182 to leucine) results in mild haemophilia BmS A Taylor, M B Liddell, I R Peake, et al.

British Journal of Haematology|March 1, 1986

Comparison of phenotypic assessment and the use of two restriction fragment length polymorphisms in the diagnosis of the carrier state in haemophilia BD P Lillicrap, M B Liddell, R J Matthews, et al.

Blood|April 1, 1991

Cosegregation of von Willebrand factor gene polymorphisms and possible germinal mosaicism in type IIB von Willebrand diseaseE W Murray, A R Giles, P J Bridge, et al.

Human Genetics|July 1, 1988

A complete deletion of the factor IX gene and new TaqI variant in a hemophilia B kindredS A Taylor, D P Lillicrap, V Blanchette, et al.

American Journal of Human Genetics|August 1, 1990

Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human geneD D Koeberl, C D Bottema, R P Ketterling, et al.

British Journal of Haematology|August 1, 1989

Factor IX Cardiff: a variant factor IX protein that shows abnormal activation is caused by an arginine to cysteine substitution at position 145M B Liddell, I R Peake, S A Taylor, et al.

American Journal of Clinical Pathology|October 1, 1989

Absence of a bleeding tendency in severe acquired von Willebrand's disease. The role of platelet von Willebrand factor in maintaining normal hemostasisJ Drouin, D P Lillicrap, C A Izaguirre, et al.

Retina (Philadelphia, Pa.)|April 26, 2001

Prevalence of factor V Leiden and activated protein C resistance in central retinal vein occlusionT M Johnson, S El-Defrawy, W G Hodge, et al.

Blood|January 1, 1990

Variation of the non-factor VIII sequences detected by a probe from intron 22 of the factor VIII geneD P Lillicrap, S A Taylor, P C Schuringa, et al.

American Journal of Medical Genetics|March 1, 1987

Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere-fra(X)-DXS15-DXS52-F8C-telomereL M Mulligan, H J Grover, V S Blanchette, et al.

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