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6. Factor XIII Deficiency in Western Afghanistan due to a Novel F13A Gene Mutation. Mousavi SH; Zeinali S; Mesbah-Namin SA; Shams M; Dorgalaleh A Int J Lab Hematol; 2020 Feb; 42(1):e1-e3. PubMed ID: 31136071 [No Abstract] [Full Text] [Related]
7. [Molecular pathology of the b subunit deficiency for factor XIII]. Ichinose A Rinsho Byori; 1997 Feb; Suppl 104():1-6. PubMed ID: 9128357 [No Abstract] [Full Text] [Related]
9. An electrophoretic and quantitative analysis of coagulation factor XIII in normal and deficient subjects. Board PG; Coggan M; Hamer JW Br J Haematol; 1980 Aug; 45(4):633-40. PubMed ID: 7426441 [TBL] [Abstract][Full Text] [Related]
10. The normal and abnormal genes of the a and b subunits in coagulation factor XIII. Ichinose A; Izumi T; Hashiguchi T Semin Thromb Hemost; 1996; 22(5):385-91. PubMed ID: 8989821 [TBL] [Abstract][Full Text] [Related]
11. Haplotypes of the coagulation factor XIII A subunit locus in normal and deficient subjects. Board PG; Chapple R; Coggan M Am J Hum Genet; 1988 May; 42(5):712-7. PubMed ID: 2895980 [TBL] [Abstract][Full Text] [Related]
12. Quality of life of people with hereditary factor XIII deficiency treated at a reference centre. Drumond A; Camelo RM Haemophilia; 2021 Sep; 27(5):e649-e653. PubMed ID: 34329524 [No Abstract] [Full Text] [Related]
13. Factor XIII deficiency. A family study by measurement of factor XIII subunits A and S. Francis JL; Todd PJ Acta Haematol; 1979; 62(3):167-72. PubMed ID: 118616 [TBL] [Abstract][Full Text] [Related]
14. Factor XIII mutation spectrum in Iranian patients with hereditary factor XIII deficiency: Detection of 3 novel mutations. Mirakhorli M; Behboudi Farahbakhsh F; Reza Baghaipour M; Mahmoudi T; Jazebi M; Tabatabaei SM; Aala F Int J Lab Hematol; 2019 Jun; 41(3):e61-e65. PubMed ID: 30578706 [No Abstract] [Full Text] [Related]
15. Factor XIII deficiency: an update. Schroeder V; Kohler HP Semin Thromb Hemost; 2013 Sep; 39(6):632-41. PubMed ID: 23929307 [TBL] [Abstract][Full Text] [Related]
17. Gene defects in congenital factor XIII deficiency. Mikkola H; Palotie A Semin Thromb Hemost; 1996; 22(5):393-8. PubMed ID: 8989822 [TBL] [Abstract][Full Text] [Related]
18. Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations. Katona É; Muszbek L; Devreese K; Kovács KB; Bereczky Z; Jonkers M; Shemirani AH; Mondelaers V; Ermens AA Haemophilia; 2014 Jan; 20(1):114-20. PubMed ID: 24118344 [TBL] [Abstract][Full Text] [Related]
19. A novel Cys328-terminator mutant implicated in severe coagulation factor XIII deficiency: a case report. Cai R; Li Y; Wang W; Feng Q BMC Med Genet; 2020 Sep; 21(1):175. PubMed ID: 32883222 [TBL] [Abstract][Full Text] [Related]
20. [Molecular and genetic basis of deficiency and molecular abnormality of coagulation factor XIII]. Ichinose A Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):984-7. PubMed ID: 3270917 [No Abstract] [Full Text] [Related] [Next] [New Search]