Illegitimate recombination produced a duplication within the FVIII gene in a patient with mild hemophilia A.
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M. Pirastu | A. Cao | S. Murru | L. Casula | M. Pecorara | P. Mori | Letizia Casula | Stefania Murru | Mario Pecorara | Piergiorgio Mori | Antonio Cao | Mario Pirastu
[1] M. Morfini,et al. Recurrent mutations and three novel rearrangements in the factor VIII gene of hemophilia A patients of Italian descent. , 1990, Blood.
[2] C. Shoemaker,et al. Factor VIII gene and hemophilia A. , 1989, Blood.
[3] S. Antonarakis,et al. The molecular basis of hemophilia A in man. , 1988, Trends in genetics : TIG.
[4] D. Bentley,et al. Partial deletion by illegitimate recombination of the factor IX gene in a haemophilia B family with two inhibitor patients. , 1988, Molecular biology & medicine.
[5] S. Ehrlich,et al. Copy choice illegitimate DNA recombination , 1988, Cell.
[6] A. Konopka,et al. Compilation of DNA strand exchange sites for non-homologous recombination in somatic cells. , 1988, Nucleic acids research.
[7] D. Russell,et al. Duplication of seven exons in LDL receptor gene caused by Alu-Alu recombination in a subject with familial hypercholesterolemia , 1987, Cell.
[8] D. Mager,et al. A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[9] D. Russell,et al. Exon-Alu recombination deletes 5 kilobases from the low density lipoprotein receptor gene, producing a null phenotype in familial hypercholesterolemia. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[10] A. Kutlar,et al. GγAγ(δβ)°‐thalassaemia and a new form of γ globin gene triplication identified in the Yugoslavian population , 1986 .
[11] S. Ehrlich,et al. Illegitimate recombination at the replication origin of bacteriophage M13. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[12] M. Botchan,et al. Association of crossover points with topoisomerase I cleavage sites: a model for nonhomologous recombination. , 1985, Science.
[13] E. Chen,et al. Characterization of the human factor VIII gene , 1984, Nature.
[14] G. Knutson,et al. Molecular cloning of a cDNA encoding human antihaemophilic factor , 1984, Nature.
[15] N. Maeda,et al. Duplication within the haptoglobin Hp2 gene , 1984, Nature.
[16] R. Burgess,et al. Nucleotide sequence preference at rat liver and wheat germ type 1 DNA topoisomerase breakage sites in duplex SV40 DNA. , 1984, Nucleic acids research.
[17] J. Sambrook,et al. Molecular Cloning: A Laboratory Manual , 2001 .
[18] J. Maio,et al. KpnI families of long, interspersed repetitive DNAs in human and other primate genomes. , 1982, Nucleic acids research.
[19] L. Liu,et al. Recognition sites of eukaryotic DNA topoisomerase I: DNA nucleotide sequencing analysis of topo I cleavage sites on SV40 DNA. , 1982, Nucleic acids research.
[20] J. Clegg,et al. A novel α-globin gene arrangement in man , 1980, Nature.
[21] F. Sanger,et al. DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.
[22] P. Mannucci,et al. 1-DEAMINO-8-D-ARGININE VASOPRESSIN: A NEW PHARMACOLOGICAL APPROACH TO THE MANAGEMENT OF HAEMOPHILIA AND VON WILLEBRAND'S DISEASE , 1977, The Lancet.
[23] Callaway Cw,et al. Letter: Diabetic ketoacidosis. , 1974, Lancet.