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J Gitschier

Showing results (71-80 of 84) with videos related to

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American Journal of Human Genetics|May 1, 1989
An intronic region within the human factor VIII gene is duplicated within Xq28 and is homologous to the polymorphic locus DXS115 (767)M Patterson, J Gitschier, J Bloomfield, et al.
Nature Genetics|February 13, 1999
Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouseC D Vulpe, Y M Kuo, T L Murphy, et al.
American Journal of Human Genetics|March 20, 2001
Homozygosity mapping places the acrodermatitis enteropathica gene on chromosomal region 8q24.3K Wang, E W Pugh, S Griffen, et al.
Gut|January 16, 2004
Mislocalisation of hephaestin, a multicopper ferroxidase involved in basolateral intestinal iron transport, in the sex linked anaemia mouseY M Kuo, T Su, H Chen, et al.
Nucleic Acids Research|September 25, 1991
Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII geneE G Tuddenham, D N Cooper, J Gitschier, et al.
Nucleic Acids Research|September 1, 1994
Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second editionE G Tuddenham, R Schwaab, J Seehafer, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1988
Homozygous and heterozygous deletions of the von Willebrand factor gene in patients and carriers of severe von Willebrand diseaseK Y Ngo, V T Glotz, J A Koziol, et al.
Nucleic Acids Research|November 11, 1994
Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second editionE G Tuddenham, R Schwaab, J Seehafer, et al.
Biotechnology (Reading, Mass.)|January 1, 1992
Characterization of the human factor VIII gene. 1984J Gitschier, W I Wood, T M Goralka, et al.
Human Molecular Genetics|July 1, 1994
Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cellsJ P Rossiter, M Young, M L Kimberland, et al.
Pageof 9

Showing results (71-80 of 84) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|May 1, 1989
An intronic region within the human factor VIII gene is duplicated within Xq28 and is homologous to the polymorphic locus DXS115 (767)M Patterson, J Gitschier, J Bloomfield, et al.
Nature Genetics|February 13, 1999
Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouseC D Vulpe, Y M Kuo, T L Murphy, et al.
American Journal of Human Genetics|March 20, 2001
Homozygosity mapping places the acrodermatitis enteropathica gene on chromosomal region 8q24.3K Wang, E W Pugh, S Griffen, et al.
Gut|January 16, 2004
Mislocalisation of hephaestin, a multicopper ferroxidase involved in basolateral intestinal iron transport, in the sex linked anaemia mouseY M Kuo, T Su, H Chen, et al.
Nucleic Acids Research|September 25, 1991
Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII geneE G Tuddenham, D N Cooper, J Gitschier, et al.
Nucleic Acids Research|September 1, 1994
Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second editionE G Tuddenham, R Schwaab, J Seehafer, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1988
Homozygous and heterozygous deletions of the von Willebrand factor gene in patients and carriers of severe von Willebrand diseaseK Y Ngo, V T Glotz, J A Koziol, et al.
Nucleic Acids Research|November 11, 1994
Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second editionE G Tuddenham, R Schwaab, J Seehafer, et al.
Biotechnology (Reading, Mass.)|January 1, 1992
Characterization of the human factor VIII gene. 1984J Gitschier, W I Wood, T M Goralka, et al.
Human Molecular Genetics|July 1, 1994
Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cellsJ P Rossiter, M Young, M L Kimberland, et al.
Pageof 9