Literature DB >> 2395671

Tetranucleotide repeat polymorphism in the vWF gene.

H K van Amstel1, P H Reitsma.   

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Year:  1990        PMID： 2395671      PMCID： PMC332021          DOI： 10.1093/nar/18.16.4957-a

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


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  2 in total

1.  An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.

Authors:  S C Kogan; M Doherty; J Gitschier
Journal:  N Engl J Med       Date:  1987-10-15       Impact factor: 91.245

2.  Structure of the gene for human von Willebrand factor.

Authors:  D J Mancuso; E A Tuley; L A Westfield; N K Worrall; B B Shelton-Inloes; J M Sorace; Y G Alevy; J E Sadler
Journal:  J Biol Chem       Date:  1989-11-25       Impact factor: 5.157
  2 in total
  14 in total

1.  An exclusion map for pre-eclampsia: assuming autosomal recessive inheritance.

Authors:  C Hayward; J Livingstone; S Holloway; W A Liston; D J Brock
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

2.  Characterisation of 98 alleles in 105 unrelated individuals in the F8VWF gene.

Authors:  B Mercier; C Gaucher; C Mazurier
Journal:  Nucleic Acids Res       Date:  1991-09-11       Impact factor: 16.971

3.  An unexpected transmission of von Willebrand disease type 3: the first case of maternal uniparental disomy 12.

Authors:  Pierre Boisseau; Mathilde Giraud; Catherine Ternisien; Agnès Veyradier; Edith Fressinaud; Armelle Lefrancois; Stéphane Bezieau; Marc Fouassier
Journal:  Haematologica       Date:  2011-07-12       Impact factor: 9.941

4.  Genetic mapping of the beta 1 GABA receptor gene to human chromosome 4, using a tetranucleotide repeat polymorphism.

Authors:  M Dean; S Lucas-Derse; A Bolos; S J O'Brien; E F Kirkness; C M Fraser; D Goldman
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025

5.  Complex variability of intron 40 of the von Willebrand factor (vWF) gene.

Authors:  Sandra Hering; Christa Augustin; Jeanett Edelmann; Micaela Heidel; Kathrin Chamaon; Jan Dressler; Reinhard Szibor
Journal:  Int J Legal Med       Date:  2007-02-02       Impact factor: 2.686

6.  Polymerase chain reaction amplification of two polymorphic simple repeat sequences within the von Willebrand factor gene: application to family studies in von Willebrand disease.

Authors:  A M Cumming; J G Armstrong; K Pendry; A M Burn; R T Wensley
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

7.  Familial essential thrombocythemia: clinical characteristics of 11 cases in one family.

Authors:  R J Schlemper; A P van der Maas; J C Eikenboom
Journal:  Ann Hematol       Date:  1994-03       Impact factor: 3.673

8.  A de novo satellited short arm of the Y chromosome possibly resulting from an unstable translocation.

Authors:  C L Lin; L Gibson; B Pober; T L Yang-Feng
Journal:  Hum Genet       Date:  1995-11       Impact factor: 4.132

9.  Allelic associations of two polymorphic microsatellites in intron 40 of the human von Willebrand factor gene.

Authors:  S D Pena; K T de Souza; M de Andrade; R Chakraborty
Journal:  Proc Natl Acad Sci U S A       Date:  1994-01-18       Impact factor: 11.205

10.  Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort.

Authors:  Daniel J Hampshire; Adel M Abuzenadah; Ashley Cartwright; Nawal S Al-Shammari; Rachael E Coyle; Michaela Eckert; Ahlam M Al-Buhairan; Sarah L Messenger; Ulrich Budde; Türkiz Gürsel; Jørgen Ingerslev; Ian R Peake; Anne C Goodeve
Journal:  Thromb Haemost       Date:  2013-05-23       Impact factor: 5.249
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