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Thrombosis in inherited factor VII deficiency

Journal of thrombosis and haemostasis, 2003-10, Vol.1 (10), p.2153-2158

2003

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The Interleukin-1 Polymorphism, Smoking, and the Risk of Periodontal Disease in the Population-based SHIP Study

Journal of dental research, 2003-03, Vol.82 (3), p.189-193

2003

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Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene

Haemophilia : the official journal of the World Federation of Hemophilia, 2006-09, Vol.12 (5), p.479-489

2006

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Prevalence of factor V Leiden mutation in various populations

Genetic epidemiology, 1997, Vol.14 (4), p.403-411

1997

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Different numerical chromosomal aberrations detected by FISH in oropharyngeal, hypopharyngeal and laryngeal squamous cell carcinoma

Histopathology, 1999-03, Vol.34 (3), p.234-240

1999

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High prevalence of FVHR2 polymorphism in Costarician Indians who have no FVL

Thrombosis and haemostasis, 2001-06, Vol.85 (6), p.1120

2001

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A de novo translocation 46,X,t(X;15) causing haemophilia B in a girl: a case report

British journal of haematology, 1998-03, Vol.100 (4), p.750-757

1998

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LONG-TERM FVII SUBSTITUTION IN A PRETERM INFANT WITH SEVERE GASTROINTESTINAL BLEEDING AND FVII DEFICIENCY DUE TO A HOMOZYGOUS DONOR SPLICE MUTATION IVS4+1G→A

Pediatric hematology and oncology, 2006-03, Vol.23 (2), p.129-133

2006

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Differences in chromosomal aberrations between nodular and superficial spreading malignant melanoma detected by interphase cytogenetics

Laboratory investigation, 1998-07, Vol.78 (7), p.883

1998

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Relationships between homocysteine, folate and vitamin B12 levels with the methylenetetrahydrofolate reductase polymorphism, in Indians from Western Venezuela

Thrombosis and haemostasis, 2001-01, Vol.85 (1), p.186

2001

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Haemophilia B in female twins caused by a point mutation in one factor IX gene and nonrandom inactivation patterns of the X-chromosomes

Thrombosis and haemostasis, 1997-11, Vol.78 (5), p.1347

1997

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Molecular Biology and Clinical Manifestation of Hereditary Factor VII Deficiency

Seminars in thrombosis and hemostasis, 2000, Vol.26 (4), p.0393-0400

2000

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Intron 22 of factor VIII gene--a hot spot for structural aberrations causing severe hemophilia A

Blood, 1996-04, Vol.87 (7), p.3067-3068

1996

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Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V

Haematologica (Roma), 2008-08, Vol.93 (8), p.1273-1275

2008

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Factor VIII gene polymorphisms in the Asian Indian population

Haemophilia : the official journal of the World Federation of Hemophilia, 2000-11, Vol.6 (6), p.625-630

2000

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Analysis of Filament Winding Processes and Potential Equipment Technologies

Procedia CIRP, 2017, Vol.66, p.125-130

2017

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Significance of the small subtelomeric area of chromosome 1 (1p36.3) in the progression of malignant melanoma : FISH deletion screening with YAC DNA probes

Virchows Archiv : an international journal of pathology, 1999-08, Vol.435 (2), p.105-111

1999

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Severe clinical expression in X-linked Emery–Dreifuss muscular dystrophy

Neuromuscular disorders : NMD, 1999-05, Vol.9 (3), p.166-170

1999

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Large-scale screening for factor V Leiden mutation in a north-eastern German population

Haemostasis, 1996-09, Vol.26 (5), p.233

1996

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Molecular analysis of FVIII gene in severe HA patients of Costa Rica

Hämostaseologie, 2010-11, Vol.30 Suppl 1, p.S150

2010

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Elemental Composition of Natural Nanoparticles and Fine Colloids in European Forest Stream Waters and Their Role as Phosphorus Carriers

Global biogeochemical cycles, 2017-10, Vol.31 (10), p.1592-1607

2017

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Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene

Haemophilia : the official journal of the World Federation of Hemophilia, 2009-01, Vol.15 (1), p.267-280

2009

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Biochemical Indicators of Nutritional Status and Dietary Intake in Costa Rican Cabécar Indian Adolescents

Food and nutrition bulletin, 2005-03, Vol.26 (1), p.3-16

2005

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Factor V Leiden, Prothrombin Gene G20210A Variant, and Methylenetetrahydrofolate Reductase C677T Genotype in Young Adults With Ischemic Stroke

Clinical and applied thrombosis/hemostasis, 2001-10, Vol.7 (4), p.346-350

2001

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Identification of a novel large F9 gene mutation-An insertion of an Alu repeated DNA element in exon e of the factor 9 gene

Human mutation, 2000-03, Vol.15 (3), p.299-299

2000

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Thrombosis in inherited factor VII deficiency

The Interleukin-1 Polymorphism, Smoking, and the Risk of Periodontal Disease in the Population-based SHIP Study

Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene

Prevalence of factor V Leiden mutation in various populations

Different numerical chromosomal aberrations detected by FISH in oropharyngeal, hypopharyngeal and laryngeal squamous cell carcinoma

High prevalence of FVHR2 polymorphism in Costarician Indians who have no FVL

A de novo translocation 46,X,t(X;15) causing haemophilia B in a girl: a case report

LONG-TERM FVII SUBSTITUTION IN A PRETERM INFANT WITH SEVERE GASTROINTESTINAL BLEEDING AND FVII DEFICIENCY DUE TO A HOMOZYGOUS DONOR SPLICE MUTATION IVS4+1G→A

Differences in chromosomal aberrations between nodular and superficial spreading malignant melanoma detected by interphase cytogenetics

Relationships between homocysteine, folate and vitamin B12 levels with the methylenetetrahydrofolate reductase polymorphism, in Indians from Western Venezuela

Haemophilia B in female twins caused by a point mutation in one factor IX gene and nonrandom inactivation patterns of the X-chromosomes

Molecular Biology and Clinical Manifestation of Hereditary Factor VII Deficiency

Intron 22 of factor VIII gene--a hot spot for structural aberrations causing severe hemophilia A

Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V

Factor VIII gene polymorphisms in the Asian Indian population

Analysis of Filament Winding Processes and Potential Equipment Technologies

Significance of the small subtelomeric area of chromosome 1 (1p36.3) in the progression of malignant melanoma : FISH deletion screening with YAC DNA probes

Severe clinical expression in X-linked Emery–Dreifuss muscular dystrophy

Large-scale screening for factor V Leiden mutation in a north-eastern German population

Molecular analysis of FVIII gene in severe HA patients of Costa Rica

Elemental Composition of Natural Nanoparticles and Fine Colloids in European Forest Stream Waters and Their Role as Phosphorus Carriers

Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene

Biochemical Indicators of Nutritional Status and Dietary Intake in Costa Rican Cabécar Indian Adolescents

Factor V Leiden, Prothrombin Gene G20210A Variant, and Methylenetetrahydrofolate Reductase C677T Genotype in Young Adults With Ischemic Stroke

Identification of a novel large F9 gene mutation-An insertion of an Alu repeated DNA element in exon e of the factor 9 gene

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