| 1 | EEF1AL11P, F13B, RP12, RPL30P
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| Integrated genetic and physical map of the 1q31-->q32.1 region, encompassing the RP12 locus, the F13B and HF1 genes, and the EEF1AL11 and RPL30 pseudogenes.
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| van Soest S, et al.
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| Cytogenet Cell Genet 84(1-2):22-27. 1999
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| 2 | F13B
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| Type I factor XIII deficiency is caused by a genetic defect of its b subunit : insertion of triplet AAC in exon III leads to premature termination in the second Sushi domain.
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| Izumi T, et al.
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| Blood 87 : 2769-2774. 1996
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| 3 | HUS, F13B, RCA@
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| The human factor H-related gene 2 (FHR2) : structure and linkage to the coagulation factor XIIIb gene.
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| Skerka C, et al.
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| Immunogenetics 42 : 268-274. 1995
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| 4 | F13B
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| Molecular and cellular basis of deficiency of the b subunit for factor XIII secondary to a Cys430-Phe mutation in the seventh Sushi domain.
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| Hashiguchi T, et al.
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| J Clin Invest 95 : 1002-1008. 1995
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| 5 | F13B
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| A tetranucleotide repeat for the F13B locus.
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| Nishimura DY, et al.
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| Nucleic Acids Res 20 : 1167. 1992
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| 6 | F13B
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| An updated classification of factor XIII defect.
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| Girolami A, et al.
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| Br J Haematol 77 : 565-566. 1991
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| 7 | F13B, SRPX
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| Structure of transglutaminases.
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| Ichinose A, et al.
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| J Biol Chem 265 : 13411-13414. 1990
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| 8 | HUS, F13B
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| Physical linkage of the human genes coding for complement factor H and coagulation factor XIII B subunit.
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| Rey-Campos J, et al.
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| Genomics 7 : 644-646. 1990
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| 9 | F13B
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| Localization of the coagulation factor XIII B subunit gene (F13B) to chromosome bands 1q31-32.1 and restriction fragment length polymorphism at the locus.
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| Webb GC, Coggan M, Ichinose A, Board PG.
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| Hum Genet 81 : 157-160. 1989
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| 10 | F13B, REN, SPTA1
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| The B subunit of coagulation factor XIII is linked to renin and the Duffy blood group to alpha-spectrin on human chromosome 1.
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| Griffiths LR, Board PG, Zwi MB, Morris BJ, McLeod JG, Nicholson GA.
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| Hum Hered 39 : 107-109. 1989
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| 11 | PGD, PEPC, F13B
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| Linkage data on F13B, HF, and PEPC.
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| Rocha J, et al.
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| (HGM10) Cytogenet Cell Genet 51 : 1067. 1989
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| 12 | F13B, RCA@
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| Coagulation factor XIII B subunit is encoded by a gene linked to the regulator of complement activation (RCA) gene cluster in man.
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| Rodriguez de Cordoba S, Rey-Campos J, Dykes DD, McAlpine PJ, Wong P, Rubinstein P.
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| Immunogenetics 28 : 452-454. 1988
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| 13 | C1S, C1R, JK, F13B
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| Linkage of the polymorphic protein markers F13B, C1S, C1R, and blood group antigen Kidd in CEPH reference families.
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| Leppert M, et al.
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| (HGM9) Cytogenet Cell Genet 46 : 647. 1987
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| 14 | HUS, F13B
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| Human complement factor H (HF) linked to coagulation factor XIIIB (F13B).
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| Eiberg H, et al.
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| (HGM9) Cytogenet Cell Genet 46 : 610. 1987
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| 15 | F13B
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| Coagulation factor XIII : Genetic linkage studies with F13B.
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| Bender K, et al.
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| Genet Epidemiol 4 : 43-49. 1987
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| 16 | F2, F5TPH, F7, VWF, F10, F11, F12, F13A1, F13B, FG@
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| The genetics of blood coagulation.
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| Graham JB, et al.
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| Adv Hum Genet 13 : 1-65. 1983
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