A complete deletion of the factor IX gene and new TaqI variant in a hemophilia B kindred
暂无分享,去创建一个
A. Giles | B. White | D. Lillicrap | S. Taylor | J. Holden | V. Blanchette
[1] L. Mulligan,et al. A DNA marker closely linked to the factor IX (haemophilia B) gene , 1987, Human Genetics.
[2] K. Kidd,et al. Report of the committee on human gene mapping by recombinant DNA techniques. , 1988, Cytogenetics and cell genetics.
[3] S. Antonarakis. The molecular genetics of hemophilia A and B in man. Factor VIII and factor IX deficiency. , 1988, Advances in human genetics.
[4] M. Poon,et al. Hemophilia B (Christmas disease) variants and carrier detection analyzed by DNA probes. , 1987, The Journal of clinical investigation.
[5] A. Bloom,et al. Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients. , 1987, The Journal of clinical investigation.
[6] S. Antonarakis,et al. Recurrent mutations in haemophilia A give evidence for CpG mutation hotspots , 1986, Nature.
[7] M. Vidaud,et al. A de novo intragenic deletion of the potential EGF domain of the factor IX gene in a family with severe hemophilia B. , 1986, Blood.
[8] K. Kurachi,et al. An intragenic deletion of the factor IX gene in a family with hemophilia B. , 1985, The Journal of clinical investigation.
[9] J. Roberts,et al. Localization of human factor FVIII inhibitor epitopes to two polypeptide fragments. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[10] S. Antonarakis,et al. Hemophilia A. Detection of molecular defects and of carriers by DNA analysis. , 1985, The New England journal of medicine.
[11] C. Peschle,et al. Hemophilia B with inhibitor: molecular analysis of the subtotal deletion of the factor IX gene. , 1985, Blood.
[12] R. Gambari,et al. Gene deletion in an Italian haemophilia B subject. , 1985, Journal of medical genetics.
[13] K. Kurachi,et al. Nucleotide sequence of the gene for human factor IX (antihemophilic factor B). , 1985, Biochemistry.
[14] L. Mulligan,et al. Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3. , 1985, American journal of human genetics.
[15] E. Chen,et al. Detection and sequence of mutations in the factor VIII gene of haemophiliacs , 1985, Nature.
[16] D. Rees,et al. The gene structure of human anti‐haemophilic factor IX. , 1984, The EMBO journal.
[17] A. Bloom,et al. CARRIER DETECTION BY DIRECT GENE ANALYSIS IN A FAMILY WITH HAEMOPHILIA B (FACTOR IX DEFICIENCY) , 1984, The Lancet.
[18] G. Brownlee,et al. CHARACTERISATION AND USE OF AN INTRAGENIC POLYMORPHIC MARKER FOR DETECTION OF CARRIERS OF HAEMOPHILIA B (FACTOR IX DEFICIENCY) , 1984, The Lancet.
[19] E. Briët,et al. Inhibitors in Christmas disease. , 1984, Progress in clinical and biological research.
[20] D. Rees,et al. Gene deletions in patients with haemophilia B and anti-factor IX antibodies , 1983, Nature.
[21] C. Rizza,et al. Treatment of haemophilia and related disorders in Britain and Northern Ireland during 1976-80: report on behalf of the directors of haemophilia centres in the United Kingdom. , 1983, British medical journal.
[22] H. Willard,et al. Report of the committee on human gene mapping by recombinant DNA techniques. , 1982, Birth defects original article series.
[23] D. Green,et al. A More Uniform Measurement of Factor VIII Inhibitors , 1975, Thrombosis and Haemostasis.
[24] A. Imbriano. [Blood coagulation]. , 1955, La Semana medica.