 Connection
Hanna Roberts to Mutation
This is a "connection" page, showing publications Hanna Roberts has written about Mutation.
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Connection Strength |
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0.041 |
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Chaing S, Clarke B, Sridhara S, Chu K, Friedman P, VanDusen W, Roberts HR, Blajchman M, Monroe DM, High KA. Severe factor VII deficiency caused by mutations abolishing the cleavage site for activation and altering binding to tissue factor. Blood. 1994 Jun 15; 83(12):3524-35.
Score: 0.013
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Watzke HH, Lechner K, Roberts HR, Reddy SV, Welsch DJ, Friedman P, Mahr G, Jagadeeswaran P, Monroe DM, High KA. Molecular defect (Gla+14----Lys) and its functional consequences in a hereditary factor X deficiency (factor X "Vorarlberg"). J Biol Chem. 1990 Jul 15; 265(20):11982-9.
Score: 0.010
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Monroe DM, McCord DM, Huang MN, High KA, Lundblad RL, Kasper CK, Roberts HR. Functional consequences of an arginine180 to glutamine mutation in factor IX Hilo. Blood. 1989 May 01; 73(6):1540-4.
Score: 0.009
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Chung KS, Goldsmith JC, Roberts HR. Isolation and characterization of factor IX Chapel Hill: comparison to normal human factor IX. Bibl Haematol. 1977; 44:68-74.
Score: 0.004
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Brown PE, Hougie C, Roberts HR. The genetic heterogeneity of hemophilia B. N Engl J Med. 1970 Jul 09; 283(2):61-4.
Score: 0.002
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Huang MN, Kasper CK, Roberts HR, Stafford DW, High KA. Molecular defect in factor IXHilo, a hemophilia Bm variant: Arg----Gln at the carboxyterminal cleavage site of the activation peptide. Blood. 1989 Feb 15; 73(3):718-21.
Score: 0.002
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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.
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