Connection

Flora Peyvandi to Phenotype

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This is a "connection" page, showing publications Flora Peyvandi has written about Phenotype.
Flora Peyvandi
Connection Strength
0.149
Phenotype
  1. Risk of diagnostic delay in congenital thrombotic thrombocytopenic purpura. J Thromb Haemost. 2019 Apr; 17(4):666-669.
    View in: PubMed
    Score: 0.086
  2. Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency. Br J Haematol. 2002 Jun; 117(3):685-92.
    View in: PubMed
    Score: 0.027
  3. Clustered F8 missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis and activity. Haematologica. 2018 02; 103(2):344-350.
    View in: PubMed
    Score: 0.020
  4. Frequency of the p.Gly262Asp mutation in congenital Factor X deficiency. Eur J Clin Invest. 2015 Oct; 45(10):1087-91.
    View in: PubMed
    Score: 0.017
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.