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Epilepsy Research
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November 1, 1990
Stargazer: a new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures
J L Noebels, X Qiao, R T Bronson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1993
Identification and genetic mapping of the murine gene and 20 related sequences encoding chromosomal protein HMG-17
K R Johnson, S A Cook, P Ward-Bailey, et al.
Genomics
|
December 1, 1992
Genetic mapping of a new homeobox gene to mouse chromosome 7
K R Johnson, S Lu, M T Murtha, et al.
Genomics
|
May 15, 1994
The mouse congenital polycystic kidney (cpk) locus maps within 1.3 cM of the chromosome 12 marker D12Nyu2
E A Simon, S Cook, M T Davisson, et al.
Genetical Research
|
August 1, 1991
Sandy: a new mouse model for platelet storage pool deficiency
R T Swank, H O Sweet, M T Davisson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 1, 1996
Megencephaly: a new mouse mutation on chromosome 6 that causes hypertrophy of the brain
L R Donahue, S A Cook, K R Johnson, et al.
Cytometry
|
February 1, 1996
Heterogeneity of B-lymphoid tumors in E mu-myc transgenic mice
V S Prasad, M J Temple, M T Davisson, et al.
Genetical Research
|
October 1, 1990
The hairy ears (Eh) mutation is closely associated with a chromosomal rearrangement in mouse chromosome 15
M T Davisson, T H Roderick, E C Akeson, et al.
Human Molecular Genetics
|
November 1, 1994
A frameshift mutation in the mouse alpha 1 glycine receptor gene (Glra1) results in progressive neurological symptoms and juvenile death
M S Buckwalter, S A Cook, M T Davisson, et al.
The Journal of Heredity
|
December 29, 1998
A new allelic series for the underwhite gene on mouse chromosome 15
H O Sweet, M H Brilliant, S A Cook, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 139) with videos related to
Sort By:
Page
of 14
Epilepsy Research
|
November 1, 1990
Stargazer: a new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures
J L Noebels, X Qiao, R T Bronson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1993
Identification and genetic mapping of the murine gene and 20 related sequences encoding chromosomal protein HMG-17
K R Johnson, S A Cook, P Ward-Bailey, et al.
Genomics
|
December 1, 1992
Genetic mapping of a new homeobox gene to mouse chromosome 7
K R Johnson, S Lu, M T Murtha, et al.
Genomics
|
May 15, 1994
The mouse congenital polycystic kidney (cpk) locus maps within 1.3 cM of the chromosome 12 marker D12Nyu2
E A Simon, S Cook, M T Davisson, et al.
Genetical Research
|
August 1, 1991
Sandy: a new mouse model for platelet storage pool deficiency
R T Swank, H O Sweet, M T Davisson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 1, 1996
Megencephaly: a new mouse mutation on chromosome 6 that causes hypertrophy of the brain
L R Donahue, S A Cook, K R Johnson, et al.
Cytometry
|
February 1, 1996
Heterogeneity of B-lymphoid tumors in E mu-myc transgenic mice
V S Prasad, M J Temple, M T Davisson, et al.
Genetical Research
|
October 1, 1990
The hairy ears (Eh) mutation is closely associated with a chromosomal rearrangement in mouse chromosome 15
M T Davisson, T H Roderick, E C Akeson, et al.
Human Molecular Genetics
|
November 1, 1994
A frameshift mutation in the mouse alpha 1 glycine receptor gene (Glra1) results in progressive neurological symptoms and juvenile death
M S Buckwalter, S A Cook, M T Davisson, et al.
The Journal of Heredity
|
December 29, 1998
A new allelic series for the underwhite gene on mouse chromosome 15
H O Sweet, M H Brilliant, S A Cook, et al.
Page
of 14