Literature DB >> 1979312

An HhaI polymorphism is present in factor IX genes of Asian subjects.

A P Reiner1, A R Thompson.   

Abstract

Hemophilia B is caused by decreased factor IX procoagulant activity. An HhaI restriction site polymorphism near the factor IX gene has been detected by the polymerase chain reaction. Frequency and linkage data already observed in Caucasians are confirmed and the polymorphism is also prevalent in the factor IX genes of Black and Asian populations.

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Year:  1990        PMID： 1979312     DOI： 10.1007/bf00205181

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  8 in total

Review 1.  Molecular biology of the hemophilias.

Authors:  A R Thompson
Journal:  Prog Hemost Thromb       Date:  1991

2.  A new MspI restriction fragment length polymorphism in the hemophilia B locus.

Authors:  G Camerino; I Oberlé; D Drayna; J L Mandel
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  A 50 bp polymorphic insertion in the factor IX gene is readily detected by amplification and is in equilibrium with other polymorphic sites.

Authors:  D P Bouvier; S H Chen; A R Thompson
Journal:  Nucleic Acids Res       Date:  1990-09-11       Impact factor: 16.971

4.  Diagnostic role of an immunoassay-detected polymorphism of factor IX for potential carriers of hemophilia B.

Authors:  A R Thompson; S H Chen; K J Smith
Journal:  Blood       Date:  1988-11       Impact factor: 22.113

5.  Detection of polymorphisms at cytosine phosphoguanadine dinucleotides and diagnosis of haemophilia B carriers.

Authors:  P R Winship; D J Rees; M Alkan
Journal:  Lancet       Date:  1989-03-25       Impact factor: 79.321

6.  The factor IX BamHI polymorphism: T-to-G transversion at the nucleotide sequence -561. The BamHI/MSPI haplotypes in blacks and Caucasians.

Authors:  M Zhang; S H Chen; C R Scott; A R Thompson
Journal:  Hum Genet       Date:  1989-06       Impact factor: 4.132

7.  Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms.

Authors:  P R Winship; D S Anson; C R Rizza; G G Brownlee
Journal:  Nucleic Acids Res       Date:  1984-12-11       Impact factor: 16.971

8.  Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

Authors:  G Camerino; K H Grzeschik; M Jaye; H De La Salle; P Tolstoshev; J P Lecocq; R Heilig; J L Mandel
Journal:  Proc Natl Acad Sci U S A       Date:  1984-01       Impact factor: 11.205
  8 in total
  1 in total

1.  CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle series.

Authors:  S H Chen; M Zhang; E W Lovrien; C R Scott; A R Thompson
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132
  1 in total

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