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J Gitschier

Showing results (51-60 of 84) with videos related to

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American Journal of Human Genetics|August 5, 2000
Familial aggregation of absolute pitchS Baharloo, S K Service, N Risch, et al.
American Journal of Human Genetics|November 1, 1994
Diverse mutations in patients with Menkes disease often lead to exon skippingS Das, B Levinson, S Whitney, et al.
Human Mutation|January 1, 1992
Missense mutations causing mild hemophilia A in Iceland detected by denaturing gradient gel electrophoresisS Jonsdottir, C Diamond, B Levinson, et al.
Nature Structural Biology|January 23, 1998
Solution structure of the fourth metal-binding domain from the Menkes copper-transporting ATPaseJ Gitschier, B Moffat, D Reilly, et al.
American Journal of Human Genetics|May 1, 1994
Molecular evidence that the p55 gene is not responsible for either of two Xq28-linked disorders: Emery-Dreifuss muscular dystrophy and dyskeratosis congenitaA B Metzenberg, Y Pan, S Das, et al.
American Journal of Human Genetics|March 1, 1995
Similar splicing mutations of the Menkes/mottled copper-transporting ATPase gene in occipital horn syndrome and the blotchy mouseS Das, B Levinson, C Vulpe, et al.
Nature Genetics|January 1, 1993
Are X-linked cutis laxa and Menkes disease allelic?B Levinson, J Gitschier, C Vulpe, et al.
Genomics|July 11, 1992
Sequence of the human factor VIII-associated gene is conserved in mouseB Levinson, J R Bermingham, A Metzenberg, et al.
Nucleic Acids Research|May 11, 1991
A TaqI polymorphism adjacent to the factor VIII gene (F8C)S Kenwrick, P Bridge, D Lillicrap, et al.
Nature|April 1, 1985
Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII geneJ Gitschier, D Drayna, E G Tuddenham, et al.
Pageof 9

Showing results (51-60 of 84) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|August 5, 2000
Familial aggregation of absolute pitchS Baharloo, S K Service, N Risch, et al.
American Journal of Human Genetics|November 1, 1994
Diverse mutations in patients with Menkes disease often lead to exon skippingS Das, B Levinson, S Whitney, et al.
Human Mutation|January 1, 1992
Missense mutations causing mild hemophilia A in Iceland detected by denaturing gradient gel electrophoresisS Jonsdottir, C Diamond, B Levinson, et al.
Nature Structural Biology|January 23, 1998
Solution structure of the fourth metal-binding domain from the Menkes copper-transporting ATPaseJ Gitschier, B Moffat, D Reilly, et al.
American Journal of Human Genetics|May 1, 1994
Molecular evidence that the p55 gene is not responsible for either of two Xq28-linked disorders: Emery-Dreifuss muscular dystrophy and dyskeratosis congenitaA B Metzenberg, Y Pan, S Das, et al.
American Journal of Human Genetics|March 1, 1995
Similar splicing mutations of the Menkes/mottled copper-transporting ATPase gene in occipital horn syndrome and the blotchy mouseS Das, B Levinson, C Vulpe, et al.
Nature Genetics|January 1, 1993
Are X-linked cutis laxa and Menkes disease allelic?B Levinson, J Gitschier, C Vulpe, et al.
Genomics|July 11, 1992
Sequence of the human factor VIII-associated gene is conserved in mouseB Levinson, J R Bermingham, A Metzenberg, et al.
Nucleic Acids Research|May 11, 1991
A TaqI polymorphism adjacent to the factor VIII gene (F8C)S Kenwrick, P Bridge, D Lillicrap, et al.
Nature|April 1, 1985
Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII geneJ Gitschier, D Drayna, E G Tuddenham, et al.
Pageof 9