C D Bottema - JoVE Visualize

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Genomics|January 7, 1998

The mouse homeobox gene, Gbx2: genomic organization and expression in pluripotent cells in vitro and in vivoG Chapman, J L Remiszewski, G C Webb, et al.

Genomics|August 1, 1996

Structure and chromosomal localization of the genomic locus encoding the Kiz1 LIM-kinase geneO Bernard, V Burkitt, G C Webb, et al.

American Journal of Human Genetics|October 1, 1991

Missense mutations and evolutionary conservation of amino acids: evidence that many of the amino acids in factor IX function as "spacer" elementsC D Bottema, R P Ketterling, S Ii, et al.

American Journal of Human Genetics|August 1, 1990

Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human geneD D Koeberl, C D Bottema, R P Ketterling, et al.

American Journal of Human Genetics|January 1, 1993

Germ-line origins of mutation in families with hemophilia B: the sex ratio varies with the type of mutationR P Ketterling, E Vielhaber, C D Bottema, et al.

Human Genetics|June 1, 1993

The pattern of spontaneous germ-line mutation: relative rates of mutation at or near CpG dinucleotides in the factor IX geneC D Bottema, R P Ketterling, E Vielhaber, et al.

American Journal of Human Genetics|October 1, 1991

Why does the human factor IX gene have a G + C content of 40%?C D Bottema, M J Bottema, R P Ketterling, et al.

Human Molecular Genetics|March 1, 1993

Germline mutations in the factor IX gene: a comparison of the pattern in Caucasians and non-CaucasiansB Gostout, E Vielhaber, R P Ketterling, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 7, 2001

An orphaned mammalian beta-globin gene of ancient evolutionary originD Wheeler, R Hope, S B Cooper, et al.

Genomics|February 12, 1998

Structural organization of the mouse and human GALR1 galanin receptor genes (Galnr and GALNR) and chromosomal localization of the mouse geneA S Jacoby, G C Webb, M L Liu, et al.

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Showing results (21-30 of 35) with videos related to

Sort By:

Pageof 4

Genomics|January 7, 1998

The mouse homeobox gene, Gbx2: genomic organization and expression in pluripotent cells in vitro and in vivoG Chapman, J L Remiszewski, G C Webb, et al.

Genomics|August 1, 1996

Structure and chromosomal localization of the genomic locus encoding the Kiz1 LIM-kinase geneO Bernard, V Burkitt, G C Webb, et al.

American Journal of Human Genetics|October 1, 1991

Missense mutations and evolutionary conservation of amino acids: evidence that many of the amino acids in factor IX function as "spacer" elementsC D Bottema, R P Ketterling, S Ii, et al.

American Journal of Human Genetics|August 1, 1990

Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human geneD D Koeberl, C D Bottema, R P Ketterling, et al.

American Journal of Human Genetics|January 1, 1993

Germ-line origins of mutation in families with hemophilia B: the sex ratio varies with the type of mutationR P Ketterling, E Vielhaber, C D Bottema, et al.

Human Genetics|June 1, 1993

The pattern of spontaneous germ-line mutation: relative rates of mutation at or near CpG dinucleotides in the factor IX geneC D Bottema, R P Ketterling, E Vielhaber, et al.

American Journal of Human Genetics|October 1, 1991

Why does the human factor IX gene have a G + C content of 40%?C D Bottema, M J Bottema, R P Ketterling, et al.

Human Molecular Genetics|March 1, 1993

Germline mutations in the factor IX gene: a comparison of the pattern in Caucasians and non-CaucasiansB Gostout, E Vielhaber, R P Ketterling, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 7, 2001

An orphaned mammalian beta-globin gene of ancient evolutionary originD Wheeler, R Hope, S B Cooper, et al.

Genomics|February 12, 1998

Structural organization of the mouse and human GALR1 galanin receptor genes (Galnr and GALNR) and chromosomal localization of the mouse geneA S Jacoby, G C Webb, M L Liu, et al.

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