Literature DB >> 1678511

NcoI RFLP in the human prothrombin (F2) gene.

H Iwahana1, K Yoshimoto, M Itakura.   

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Year:  1991        PMID： 1678511      PMCID： PMC328599          DOI： 10.1093/nar/19.15.4309-a

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


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  1 in total

1.  Human genes encoding prothrombin and ceruloplasmin map to 11p11-q12 and 3q21-24, respectively.

Authors:  N J Royle; D M Irwin; M L Koschinsky; R T MacGillivray; J L Hamerton
Journal:  Somat Cell Mol Genet       Date:  1987-05
  1 in total
  4 in total

1.  Highly polymorphic region of the human prothrombin (F2) gene.

Authors:  H Iwahana; K Yoshimoto; M Itakura
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

2.  Detection of a new polymorphism of the human prothrombin (F2) gene by combination of PASA and mutated primer-mediated PCR-RFLP.

Authors:  H Iwahana; N Mizusawa; K Yoshimoto; M Itakura
Journal:  Hum Genet       Date:  1992-11       Impact factor: 4.132

3.  High-resolution meiotic and physical mapping of the best vitelliform macular dystrophy (VMD2) locus to pericentromeric chromosome 11.

Authors:  B H Weber; G Vogt; H Stöhr; S Sander; D Walker; C Jones
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

4.  Molecular and genetic analysis of a compound heterozygote for dysprothrombinemia of prothrombin Tokushima and hypoprothrombinemia.

Authors:  H Iwahana; K Yoshimoto; T Shigekiyo; A Shirakami; S Saito; M Itakura
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025
  4 in total

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