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M T Davisson

Showing results (91-100 of 139) with videos related to

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Genomics|August 15, 1996
Chromosomal localization of a new mouse lens opacity gene (lop18)B Chang, N L Hawes, R S Smith, et al.
Neural Networks : the Official Journal of the International Neural Network Society|March 29, 2003
Mouse chromosome classification by radial basis function network with fast orthogonal searchM T. Musavi, R J. Bryant, M Qiao, et al.
The Journal of Urology|November 1, 1988
Congenital progressive hydronephrosis in mice: a new recessive mutationC E Horton, M T Davisson, J B Jacobs, et al.
Human Molecular Genetics|June 13, 1998
A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactylyK R Johnson, H O Sweet, L R Donahue, et al.
The Journal of Heredity|July 10, 1998
Juvenile bare: a new hair loss mutation on chromosome 7 of the mouseP W Lane, R T Bronson, S A Cook, et al.
Cytogenetic and Genome Research|January 4, 2005
Report on the 'Expert Workshop on the Biology of Chromosome 21: towards gene-phenotype correlations in Down syndrome', held June 11-14, 2004, Washington D.CK Gardiner, M T Davisson, M Pritchard, et al.
Biochemical Genetics|August 1, 1976
Evolution of mammalian carbonic anhydrase loci by tanden duplication: close linkage of Car-1 and Car-2 to the centromere region of chromosome 3 of the mouseE M Eicher, R H Stern, J E Womack, et al.
The Journal of Endocrinology|April 1, 1994
Adrenocortical dysplasia: a mouse model system for adrenocortical insufficiencyW G Beamer, H O Sweet, R T Bronson, et al.
Immunogenetics|January 1, 1989
The mouse mutation severe combined immune deficiency (scid) is on chromosome 16G C Bosma, M T Davisson, N R Ruetsch, et al.
Biochemical Genetics|October 1, 1986
Differences in the metabolism of the aromatic amino acid hydroxylase cofactor, tetrahydrobiopterin, in mutant mice with neurological and immunological defectsD S Duch, S W Bowers, J H Woolf, et al.
Pageof 14

Showing results (91-100 of 139) with videos related to

Sort By:
Pageof 14
Genomics|August 15, 1996
Chromosomal localization of a new mouse lens opacity gene (lop18)B Chang, N L Hawes, R S Smith, et al.
Neural Networks : the Official Journal of the International Neural Network Society|March 29, 2003
Mouse chromosome classification by radial basis function network with fast orthogonal searchM T. Musavi, R J. Bryant, M Qiao, et al.
The Journal of Urology|November 1, 1988
Congenital progressive hydronephrosis in mice: a new recessive mutationC E Horton, M T Davisson, J B Jacobs, et al.
Human Molecular Genetics|June 13, 1998
A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactylyK R Johnson, H O Sweet, L R Donahue, et al.
The Journal of Heredity|July 10, 1998
Juvenile bare: a new hair loss mutation on chromosome 7 of the mouseP W Lane, R T Bronson, S A Cook, et al.
Cytogenetic and Genome Research|January 4, 2005
Report on the 'Expert Workshop on the Biology of Chromosome 21: towards gene-phenotype correlations in Down syndrome', held June 11-14, 2004, Washington D.CK Gardiner, M T Davisson, M Pritchard, et al.
Biochemical Genetics|August 1, 1976
Evolution of mammalian carbonic anhydrase loci by tanden duplication: close linkage of Car-1 and Car-2 to the centromere region of chromosome 3 of the mouseE M Eicher, R H Stern, J E Womack, et al.
The Journal of Endocrinology|April 1, 1994
Adrenocortical dysplasia: a mouse model system for adrenocortical insufficiencyW G Beamer, H O Sweet, R T Bronson, et al.
Immunogenetics|January 1, 1989
The mouse mutation severe combined immune deficiency (scid) is on chromosome 16G C Bosma, M T Davisson, N R Ruetsch, et al.
Biochemical Genetics|October 1, 1986
Differences in the metabolism of the aromatic amino acid hydroxylase cofactor, tetrahydrobiopterin, in mutant mice with neurological and immunological defectsD S Duch, S W Bowers, J H Woolf, et al.
Pageof 14