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C M Abbott

Showing results (11-20 of 36) with videos related to

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Molecular Microbiology|January 29, 2000
Two opposing effects of mismatch repair on CTG repeat instability in Escherichia coliK H Schmidt, C M Abbott, D R Leach
Genomics|October 13, 2001
Comparative genomic analysis of genes encoding translation elongation factor 1B(alpha) in human and mouse shows EEF1B1 to be a recent retrotransposition eventD M Chambers, G A Rouleau, C M Abbott
Genetics|December 1, 1996
Genetic and physical mapping of the mouse Ulnaless locusC L Peichel, C M Abbott, T F Vogt
Annals of Human Genetics|October 1, 1992
The genes coding for phosphoenolpyruvate carboxykinase-1 (PCK1) and neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) map to human chromosome 20, extending the known region of homology with mouse chromosome 2A J Pilz, E Willer, S Povey, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Mapping of the human homologs of the murine paired-box-containing genesA J Pilz, S Povey, P Gruss, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1986
Deficiency of adenosine deaminase in the wasted mouseC M Abbott, C J Skidmore, A G Searle, et al.
Lancet (London, England)|April 2, 1988
Prenatal diagnosis of alpha-1-antitrypsin deficiency using polymerase chain reactionC M Abbott, C J McMahon, D B Whitehouse, et al.
Biochemical and Biophysical Research Communications|September 15, 1998
Evaluation of Lama5 as a candidate for the mouse ragged (Ra) mutationM E Durkin, R Albrechtsen, D M Chambers, et al.
Prenatal Diagnosis|June 1, 1993
Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 casesC M Abbott, J U Lovegrove, D B Whitehouse, et al.
Prenatal Diagnosis|April 1, 1992
Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 casesC M Abbott, J U Lovegrove, D B Whitehouse, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Molecular Microbiology|January 29, 2000
Two opposing effects of mismatch repair on CTG repeat instability in Escherichia coliK H Schmidt, C M Abbott, D R Leach
Genomics|October 13, 2001
Comparative genomic analysis of genes encoding translation elongation factor 1B(alpha) in human and mouse shows EEF1B1 to be a recent retrotransposition eventD M Chambers, G A Rouleau, C M Abbott
Genetics|December 1, 1996
Genetic and physical mapping of the mouse Ulnaless locusC L Peichel, C M Abbott, T F Vogt
Annals of Human Genetics|October 1, 1992
The genes coding for phosphoenolpyruvate carboxykinase-1 (PCK1) and neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) map to human chromosome 20, extending the known region of homology with mouse chromosome 2A J Pilz, E Willer, S Povey, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
Mapping of the human homologs of the murine paired-box-containing genesA J Pilz, S Povey, P Gruss, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1986
Deficiency of adenosine deaminase in the wasted mouseC M Abbott, C J Skidmore, A G Searle, et al.
Lancet (London, England)|April 2, 1988
Prenatal diagnosis of alpha-1-antitrypsin deficiency using polymerase chain reactionC M Abbott, C J McMahon, D B Whitehouse, et al.
Biochemical and Biophysical Research Communications|September 15, 1998
Evaluation of Lama5 as a candidate for the mouse ragged (Ra) mutationM E Durkin, R Albrechtsen, D M Chambers, et al.
Prenatal Diagnosis|June 1, 1993
Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 casesC M Abbott, J U Lovegrove, D B Whitehouse, et al.
Prenatal Diagnosis|April 1, 1992
Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 casesC M Abbott, J U Lovegrove, D B Whitehouse, et al.
Pageof 4