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Progress in Clinical and Biological Research
|
January 1, 1993
Segmental trisomy as a mouse model for Down syndrome
M T Davisson, C Schmidt, R H Reeves, et al.
American Journal of Human Genetics
|
September 28, 2001
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4
J M Newton, O Cohen-Barak, N Hagiwara, et al.
Cytogenetics and Cell Genetics
|
January 1, 1979
Report of the committee on comparative mapping
P L Pearson, T H Roderick, M T Davisson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
August 1, 1995
Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophy
D S Rice, R W Williams, P Ward-Bailey, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1992
Comparative map for mice and humans
J H Nadeau, M T Davisson, D P Doolittle, et al.
Birth Defects Original Article Series
|
January 1, 1980
Report of the committee on comparative mapping
P L Pearson, T H Roderick, M T Davisson, et al.
Cytogenetics and Cell Genetics
|
January 1, 1988
Report of the committee on comparative mapping
P A Lalley, M T Davisson, J A Graves, et al.
The Journal of Biological Chemistry
|
May 15, 1989
The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities
C A Langner, E H Birkenmeier, O Ben-Zeev, et al.
Genomics
|
July 20, 1995
RNA expression and chromosomal location of the mouse long-chain acyl-CoA dehydrogenase gene
M E Hinsdale, S C Farmer, K R Johnson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 29, 2000
Grey intense: a new mouse mutation affecting pigmentation
M T Davisson, K R Johnson, R T Bronson, et al.
Page
of 14
Search research articles
Search
Showing results (111-120 of 139) with videos related to
Sort By:
Page
of 14
Progress in Clinical and Biological Research
|
January 1, 1993
Segmental trisomy as a mouse model for Down syndrome
M T Davisson, C Schmidt, R H Reeves, et al.
American Journal of Human Genetics
|
September 28, 2001
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4
J M Newton, O Cohen-Barak, N Hagiwara, et al.
Cytogenetics and Cell Genetics
|
January 1, 1979
Report of the committee on comparative mapping
P L Pearson, T H Roderick, M T Davisson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
August 1, 1995
Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophy
D S Rice, R W Williams, P Ward-Bailey, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1992
Comparative map for mice and humans
J H Nadeau, M T Davisson, D P Doolittle, et al.
Birth Defects Original Article Series
|
January 1, 1980
Report of the committee on comparative mapping
P L Pearson, T H Roderick, M T Davisson, et al.
Cytogenetics and Cell Genetics
|
January 1, 1988
Report of the committee on comparative mapping
P A Lalley, M T Davisson, J A Graves, et al.
The Journal of Biological Chemistry
|
May 15, 1989
The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities
C A Langner, E H Birkenmeier, O Ben-Zeev, et al.
Genomics
|
July 20, 1995
RNA expression and chromosomal location of the mouse long-chain acyl-CoA dehydrogenase gene
M E Hinsdale, S C Farmer, K R Johnson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 29, 2000
Grey intense: a new mouse mutation affecting pigmentation
M T Davisson, K R Johnson, R T Bronson, et al.
Page
of 14