141 related articles for article (PubMed ID: 3454378)
1. Gene dosage effects for coagulation factors XII (F12) and XIII subunit A (F13A) in a case of partial monosomy 6p resulting from a maternal pericentric inversion of chromosome 6.
Narahara K; Seno Y; Nishibayashi Y; Hiramoto K; Nanba H; Kikkawa K; Kimoto H
Jinrui Idengaku Zasshi; 1987 Dec; 32(4):305-10. PubMed ID: 3454378
[No Abstract] [Full Text] [Related]
2. 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]
3. [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]
4. Ring chromosome 6: report of a patient and literature review.
Chitayat D; Hahm SY; Iqbal MA; Nitowsky HM
Am J Med Genet; 1987 Jan; 26(1):145-51. PubMed ID: 3544845
[TBL] [Abstract][Full Text] [Related]
5. Application of HUMF13A01 (AAAG)n STR polymorphism to the genetic diagnosis of coagulation factor XIII deficiency.
Kangsadalampai S; Coggan M; Caglayan SH; Aktuglu G; Board PG
Thromb Haemost; 1996 Dec; 76(6):879-82. PubMed ID: 8972004
[TBL] [Abstract][Full Text] [Related]
6. Novel deleterious mutation in the F12 gene in a Korean family with severe coagulation factor XII deficiency.
Kim HJ; Kim HJ; Kwon EH; Lee KO; Park IA; Kim SH
Blood Coagul Fibrinolysis; 2010 Oct; 21(7):683-6. PubMed ID: 20729721
[TBL] [Abstract][Full Text] [Related]
7. [The genetics of factor XII deficiency].
Kempter B; Rüth S; Epple I; Lohse P
Beitr Infusionsther; 1993; 31():174-8. PubMed ID: 7693250
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Novel deletion and insertion mutations cause splicing defects, leading to severe reduction in mRNA levels of the A subunit in severe factor XIII deficiency.
Izumi T; Nagaoka U; Saito T; Takamatsu J; Saito H; Ichinose A
Thromb Haemost; 1998 Mar; 79(3):479-85. PubMed ID: 9531026
[TBL] [Abstract][Full Text] [Related]
10. A novel mutation in a patient with congenital coagulation factor XII deficiency.
Feng Y; Ye X; Pang Y; Dai J; Wang XF; Zhou XH
Chin Med J (Engl); 2008 Jul; 121(13):1241-4. PubMed ID: 18710647
[No Abstract] [Full Text] [Related]
11. Further evidence of heterogeneity of gene defects in Italian families with factor XIII deficiency.
Castaman G; Giacomelli SH; Schroeder V; Sanna S; Valdrè L; Morfini M; Banov L; Kohler HP; Rodeghiero F
Haemophilia; 2012 Jan; 18(1):e6-8. PubMed ID: 21812861
[No Abstract] [Full Text] [Related]
12. [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]
13. 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]
14. [Characterization of a large deletion that leads to congenital factor XIII deficiency].
Otaki M; Inaba H; Shinozawa K; Fujita S; Amano K; Fukutake K
Rinsho Byori; 2008 Mar; 56(3):187-94. PubMed ID: 18411802
[TBL] [Abstract][Full Text] [Related]
15. [Molecular mechanisms of two novel mutations of factor XIII gene resulting in hereditary coagulation deficiency].
Duan BH; Wang HL; Wang XF; Hu YQ; Chu HY; Wang H; Yin J; Guo XM; Fu QH; Wu WM; Ding QL; Fang Y; Wang WB; Zhou RF; Kang WY; Xie S; Wang ZY
Zhonghua Yi Xue Za Zhi; 2003 Dec; 83(24):2158-61. PubMed ID: 14720426
[TBL] [Abstract][Full Text] [Related]
16. Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutations.
Ivaskevicius V; Windyga J; Baran B; Schroeder V; Junen J; Bykowska K; Seifried E; Kohler HP; Oldenburg J
Haemophilia; 2007 Sep; 13(5):649-57. PubMed ID: 17880458
[TBL] [Abstract][Full Text] [Related]
17. Localization of the coagulation factor XIII A subunit gene (F13A) to chromosome bands 6p24----p25.
Board PG; Webb GC; McKee J; Ichinose A
Cytogenet Cell Genet; 1988; 48(1):25-7. PubMed ID: 2903011
[TBL] [Abstract][Full Text] [Related]
18. Deficiency of coagulation factor XIII A subunit caused by the dinucleotide deletion at the 5' end of exon III.
Kamura T; Okamura T; Murakawa M; Tsuda H; Teshima T; Shibuya T; Harada M; Niho Y
J Clin Invest; 1992 Aug; 90(2):315-9. PubMed ID: 1644910
[TBL] [Abstract][Full Text] [Related]
19. Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect.
Louhichi N; Medhaffar M; Hadjsalem I; Mkaouar-Rebai E; Fendri-Kriaa N; Kanoun H; Yaïch F; Souissi T; Elloumi M; Fakhfakh F
Ann Hematol; 2010 May; 89(5):499-504. PubMed ID: 19937244
[TBL] [Abstract][Full Text] [Related]
20. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3).
Asano T; Ikeuchi T; Shinohara T; Enokido H; Hashimoto K
Jinrui Idengaku Zasshi; 1991 Sep; 36(3):257-65. PubMed ID: 1753439
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]