Literature DB >> 3865148

Polymorphism associated with the human coagulation factor X (F10) gene.

M Jaye, G Ricca, R Kaplan, R Howk, R Mudd, K Y Ngo, D S Fair, W Drohan.   

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Year:  1985        PMID： 3865148      PMCID： PMC322127          DOI： 10.1093/nar/13.22.8286

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


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  2 in total

1.  Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34).

Authors:  R A Pfeiffer; R Ott; S Gilgenkrantz; P Alexandre
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

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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