Literature DB >> 14435675

Congenital vascular defect associated with platelet abnormality and antihemophilic factor deficiency.

G RACCUGLIA, J V NEEL.   

Abstract

Entities:  

Keywords:  HEMOPHILIA/genetics; HEMORRHAGIC DIATHESIS/genetics

Mesh：

Substances：

Year:  1960        PMID： 14435675

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  4 in total

1.  Von Wllebrands disease. Distinction from other syndromes associated with a long bleeding time, and from hemophilia.

Authors: 
Journal:  Calif Med       Date:  1969-08

Review 2.  Genetics of human blood coagulation.

Authors:  C B Kerr
Journal:  J Med Genet       Date:  1965-12       Impact factor: 6.318

3.  Detection of heterozygotes in both parents of homozygous patients with Von Willebrand's disease.

Authors:  Y Sultan; J Simeon; J P Caen
Journal:  J Clin Pathol       Date:  1975-04       Impact factor: 3.411

4.  Antihaemophilic factor deficiency, capillary defect of von Willebrand type, and idiopathic thrombocytopenia occurring in one family.

Authors:  E K BLACKBURN; J M MACFIE; J H MONAGHAN; A P PAGE
Journal:  J Clin Pathol       Date:  1961-09       Impact factor: 3.411
  4 in total

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