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5. Clinical and physiologic studies of two siblings with prekallikrein (Fletcher factor) deficiency. Hathaway WE; Wuepper KD; Weston WL; Humbert JR; Rivers RP; Genton E; August CS; Montgomery RR; Mass MF Am J Med; 1976 May; 60(5):654-64. PubMed ID: 1020754 [TBL] [Abstract][Full Text] [Related]
6. Regional enteritis: evidence for genetic transmission by HLA typing. Schwartz SE; Siegelbaum SP; Fazio TL; Hubbell C; Henry JB Ann Intern Med; 1980 Sep; 93(3):424-7. PubMed ID: 7436159 [TBL] [Abstract][Full Text] [Related]
7. Linkage and association between HLA and 21-hydroxylase deficiency. Klouda PT; Harris R; Price DA J Med Genet; 1980 Oct; 17(5):337-41. PubMed ID: 7218273 [TBL] [Abstract][Full Text] [Related]
8. HLA in a selective aldosterone biosynthetic defect due to type 2 corticosterone methyl-oxidase deficiency. Brautbar C; Theodor R; Sack J; Levene C; Dupont B; Levine LS; Sharon R; Smaller S; Cohen T; Rösler A Tissue Antigens; 1981 Feb; 17(2):212-6. PubMed ID: 7233416 [TBL] [Abstract][Full Text] [Related]
9. Fletcher factor deficiency (Report of a new case). Colla G; Carrea M; Sbaffi A Ric Clin Lab; 1983; 13(4):443-8. PubMed ID: 6558774 [TBL] [Abstract][Full Text] [Related]
10. Fletcher factor deficiency--detection of a severe case in a population survey. Essien EM; Ebhota MI Acta Haematol; 1977; 58(6):353-8. PubMed ID: 413313 [TBL] [Abstract][Full Text] [Related]
11. The old and the new in prekallikrein deficiency: historical context and a family from Argentina with PK deficiency due to a new mutation (Arg541Gln) in exon 14 associated with a common polymorphysm (Asn124Ser) in exon 5. Girolami A; Vidal J; Sabagh M; Gervan N; Parody M; Peroni E; Sambado L; Guglielmone H Semin Thromb Hemost; 2014 Jul; 40(5):592-9. PubMed ID: 25075649 [TBL] [Abstract][Full Text] [Related]
12. Plasma prekallikrein (Fletcher factor) deficiency in a patient with chronic lymphocytic leukemia. Waddell CC; Brown JA; Udden MM South Med J; 1980 Dec; 73(12):1653-5. PubMed ID: 6905267 [TBL] [Abstract][Full Text] [Related]
13. Evidence for linkage between HL-A histocompatibility genes and those involved in the synthesis of the second component of complement. Fu SM; Kunkel HG; Brusman HP; Allen FH; Fotino M J Exp Med; 1974 Oct; 140(4):1108-11. PubMed ID: 4427089 [TBL] [Abstract][Full Text] [Related]
14. Duffy locus linkage and HLA antigens in hereditary motor-sensory neuropathy. Nevsímalová S; Prazák J; Herzog P; Seemanová E Schweiz Arch Neurol Psychiatr (1985); 1991; 142(1):19-29. PubMed ID: 1709295 [TBL] [Abstract][Full Text] [Related]
15. [Severe prekallikrein deficiency due to a compound heterozygosis in the KLKB1-gene]. Maak B; Kochhan L; Heuchel P; Jenderny J Hamostaseologie; 2009 May; 29(2):187-9. PubMed ID: 19404525 [TBL] [Abstract][Full Text] [Related]
17. Characterization of a recombinant that locates the hereditary hemochromatosis gene telomeric to HLA-F. Calandro LM; Baer DM; Sensabaugh GF Hum Genet; 1995 Sep; 96(3):339-42. PubMed ID: 7649553 [TBL] [Abstract][Full Text] [Related]
18. Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing. Jackson JF; Currier RD; Terasaki PI; Morton NE N Engl J Med; 1977 May; 296(20):1138-41. PubMed ID: 857157 [TBL] [Abstract][Full Text] [Related]
19. [Genetic control of mixed lymphocyte culture]. Hajek-Rosenmayr A Wien Klin Wochenschr; 1980 Dec; 92(23):834-40. PubMed ID: 6242847 [TBL] [Abstract][Full Text] [Related]
20. Prekallikrein deficiency in a kindred with kininogen deficiency and Fitzgerald trait clotting defect. Evidence that high molecular weight kininogen and prekallikrein exist as a complex in normal human plasma. Donaldson VH; Kleniewski J; Saito H; Sayed JK J Clin Invest; 1977 Sep; 60(3):571-83. PubMed ID: 893663 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]