Literature DB >> 3014443

RFLPs for PstI and EcoRI in the human blood clotting factor X gene.

C W Hay, K A Robertson, M R Fung, R T MacGillivray.   

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Year:  1986        PMID： 3014443      PMCID： PMC311520          DOI： 10.1093/nar/14.12.5118

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


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  2 in total

1.  The structural gene for human coagulation factor X is located on chromosome 13q34.

Authors:  P J Scambler; R Williamson
Journal:  Cytogenet Cell Genet       Date:  1985

2.  Characterization of an almost full-length cDNA coding for human blood coagulation factor X.

Authors:  M R Fung; C W Hay; R T MacGillivray
Journal:  Proc Natl Acad Sci U S A       Date:  1985-06       Impact factor: 11.205
  2 in total
  1 in total

1.  Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicism.

Authors:  K Wieland; D S Millar; C B Grundy; R S Mibashan; V V Kakkar; D N Cooper
Journal:  Hum Genet       Date:  1991-01       Impact factor: 4.132
  1 in total

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