Literature DB >> 2891107

A second Xba I polymorphic site within the human von Willebrand factor (vWF) gene.

J M Lavergne1, B R Bahnak, C L Verweij, H Pannekoek, D Meyer.   

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Year:  1987        PMID: 2891107      PMCID: PMC306445          DOI: 10.1093/nar/15.21.9099

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


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  3 in total

1.  Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization.

Authors:  D Ginsburg; R I Handin; D T Bonthron; T A Donlon; G A Bruns; S A Latt; S H Orkin
Journal:  Science       Date:  1985-06-21       Impact factor: 47.728

2.  RFLP for a human von Willebrand factor (vWF) cDNA clone, pvWF1100.

Authors:  C L Verweij; M Hofker; R Quadt; E Briet; H Pannekoek
Journal:  Nucleic Acids Res       Date:  1985-11-25       Impact factor: 16.971

3.  A polymorphic Xba I site within the human von Willebrand factor (vWF) gene identified by a vWF cDNA clone.

Authors:  R Quadt; C L Verweij; C J de Vries; E Briët; H Pannekoek
Journal:  Nucleic Acids Res       Date:  1986-09-11       Impact factor: 16.971

  3 in total
  3 in total

1.  Genetic and blood coagulation characterization of "Swedish" families with von Willebrand's disease types I and III: new aspects of heredity.

Authors:  M Anvret; M Blombäck; M Lindstedt; E Söderlind; M Tapper-Persson; A C Thelander
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

2.  Genetic heterogeneity of severe von Willebrand disease type III in the German population.

Authors:  R Schneppenheim; S Krey; F Bergmann; D Bock; U Budde; M Lange; R Linde; U Mittler; E Meili; G Mertes
Journal:  Hum Genet       Date:  1994-12       Impact factor: 4.132

3.  Additional markers for genetic diagnosis of type 3 von Willebrand disease in Indian population.

Authors:  Priyanka Kasatkar; Kanjaksha Ghosh; Shrimati Shetty
Journal:  Indian J Med Res       Date:  2015-12       Impact factor: 2.375

  3 in total

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