Found: 17
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Factor XIII<sub>A</sub> subunit deficiency due to a homozygous 13-base pair deletion in exon 3 of the A subunit gene.
- Published in:
- American Journal of Hematology, 1996, v. 53, n. 2, p. 77, doi. 10.1002/(SICI)1096-8652(199610)53:2<77::AID-AJH4>3.0.CO;2-0
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- Article
Diagnosis of Haemophilia in Pakistan: Current Picture.
- Published in:
- Journal of the College of Physicians & Surgeons Pakistan, 2013, v. 23, n. 6, p. 450
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- Publication type:
- Article
The prevalence of the cysteine1584 variant of von Willebrand factor is increased in type 1 von Willebrand disease: co-segregation with increased susceptibility to ADAMTS13 proteolysis but not clinical phenotype.
- Published in:
- British Journal of Haematology, 2005, v. 128, n. 6, p. 830, doi. 10.1111/j.1365-2141.2005.05375.x
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- Article
A single, multiplex analysis for all relevant activating NRAS gene mutations using heteroduplex generators.
- Published in:
- British Journal of Haematology, 2004, v. 126, n. 4, p. 602, doi. 10.1111/j.1365-2141.2004.05079.x
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- Article
correspondence Response to Langlois et al (LE 01059).
- Published in:
- 2004
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- Publication type:
- Letter
Haptoglobin type neither influences iron accumulation in normal subjects nor predicts clinical presentation in HFE C282Y haemochromatosis: phenotype and genotype analysis.
- Published in:
- British Journal of Haematology, 2003, v. 122, n. 2, p. 326, doi. 10.1046/j.1365-2141.2003.04436.x
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- Article
Identification and characterization of a novel gene encoding a SEREX antigen in chronic myeloid leukaemia.
- Published in:
- British Journal of Haematology, 2002, v. 119, n. 1, p. 112, doi. 10.1046/j.1365-2141.2002.03775.x
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- Article
High concentrations of coagulation factor VIII and thrombosis: is the factor VIII-binding domain of von Willebrand factor implicated?
- Published in:
- British Journal of Haematology, 2001, v. 113, n. 3, p. 655, doi. 10.1046/j.1365-2141.2001.02830.x
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- Publication type:
- Article
A new polymorphism in the human factor VIII gene: implications for linkage analysis in haemophilia A and for the evolution of int22h sequences.
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- British Journal of Haematology, 2000, v. 111, n. 2, p. 544, doi. 10.1046/j.1365-2141.2000.02373.x
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- Article
Linkage analysis in haemophilia A: simultaneous genotyping of two polymorphisms of the human factor VIII gene using induced heteroduplex formation.
- Published in:
- Haemophilia, 1998, v. 4, n. 6, p. 812, doi. 10.1046/j.1365-2516.1998.00202.x
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- Article
von Willebrand Factor Proteolysis by ADAMTS13.
- Published in:
- Journal of Coagulation Disorders, 2010, v. 2, n. 2, p. 1
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- Publication type:
- Article
von Willebrand Factor Proteolysis by ADAMTS13.
- Published in:
- Journal of Coagulation Disorders, 2009, v. 1, n. 1, p. 1
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- Publication type:
- Article
Specific analysis of the intron 22 XbaI polymorphism of the human factor VIII gene using long-distance PCR.
- Published in:
- British Journal of Haematology, 1999, v. 107, n. 3, p. 566, doi. 10.1046/j.1365-2141.1999.01731.x
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- Article
Factor V Leiden and the common haemochromatosis mutation HFE C282Y: is there an association in familial venous thromboembolic disease?
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- British Journal of Haematology, 1999, v. 107, n. 1, p. 210, doi. 10.1046/j.1365-2141.1999.01663.x
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- Article
Rapid genetic screening for haemochromatosis using heteroduplex technology.
- Published in:
- British Journal of Haematology, 1997, v. 98, n. 4, p. 856, doi. 10.1046/j.1365-2141.1997.3193136.x
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- Article
Factor XIII<sub>A calgary</sub>: a candidate missense mutation (Leu667Pro) in the beta barrel 2 domain of the factor XIII<sub>A</sub> subunit.
- Published in:
- British Journal of Haematology, 1995, v. 91, n. 2, p. 452, doi. 10.1111/j.1365-2141.1995.tb05321.x
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- Article
New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105.
- Published in:
- Human Molecular Genetics, 1995, v. 4, n. 10, p. 1869
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- Publication type:
- Article