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Results of search for 'au:"Davisson, M"', page 7 of 8
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Authors
Akeson, E C
Blake, J A
Bronson, R T
Chang, B
Cook, S A
Davisson, M
Davisson, M T
Donahue, L R
Eppig, J T
Harris, B S
Hawes, N L
Heckenlively, J R
John, S W
Johnson, K R
Lalley, P A
O'Brien, S J
Richardson, J E
Roderick, T H
Smith, R S
Sweet, H O
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Topics
Animals
Base Sequence
Chromosome Mapping
Chromosomes
Crosses, Genetic
Disease Models, Animal
Female
Genetic Linkage
Genetic Markers
Humans
Male
Mice
Mice, Inbred C57BL
Mice, Inbred Strains
Mice, Mutant Strains
Mutation
Phenotype
Species Specificity
genetics
pathology
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English
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121.
Effect of the mouse scid mutation on meiotic recombination.
[electronic resource]
by
Heine, D
Passmore, H C
Patel, V
Shultz, L D
Ward-Bailey, P
Cook, S A
Davisson, M T
Producer:
19961021
In:
Mammalian genome : official journal of the International Mammalian Genome Society
vol. 7
Online resources:
Available from publisher's website
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122.
Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouse.
[electronic resource]
by
Chang, B
Hawes, N L
Roderick, T H
Smith, R S
Heckenlively, J R
Horwitz, J
Davisson, M T
Producer:
19991004
In:
Molecular vision
vol. 5
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123.
Comparative map for mice and humans.
[electronic resource]
by
Nadeau, J H
Davisson, M T
Doolittle, D P
Grant, P
Hillyard, A L
Kosowsky, M R
Roderick, T H
Producer:
19921123
In:
Mammalian genome : official journal of the International Mammalian Genome Society
vol. 3
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124.
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4.
[electronic resource]
by
Newton, J M
Cohen-Barak, O
Hagiwara, N
Gardner, J M
Davisson, M T
King, R A
Brilliant, M H
Producer:
20011207
In:
American journal of human genetics
vol. 69
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125.
Report of the committee on comparative mapping.
[electronic resource]
by
Pearson, P L
Roderick, T H
Davisson, M T
Garver, J J
Warburton, D
Lalley, P A
O'Brien, S J
Producer:
19800627
In:
Cytogenetics and cell genetics
vol. 25
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126.
A standardized nomenclature for endogenous mouse mammary tumor viruses.
[electronic resource]
by
Kozak, C
Peters, G
Pauley, R
Morris, V
Michalides, R
Dudley, J
Green, M
Davisson, M
Prakash, O
Vaidya, A
Producer:
19870526
In:
Journal of virology
vol. 61
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127.
Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophy.
[electronic resource]
by
Rice, D S
Williams, R W
Ward-Bailey, P
Johnson, K R
Harris, B S
Davisson, M T
Goldowitz, D
Producer:
19960325
In:
Mammalian genome : official journal of the International Mammalian Genome Society
vol. 6
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128.
Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of reelin.
[electronic resource]
by
Goldowitz, D
Cushing, R C
Laywell, E
D'Arcangelo, G
Sheldon, M
Sweet, H O
Davisson, M
Steindler, D
Curran, T
Producer:
19971208
In:
The Journal of neuroscience : the official journal of the Society for Neuroscience
vol. 17
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129.
Report of the committee on comparative mapping.
[electronic resource]
by
Pearson, P L
Roderick, T H
Davisson, M T
Garver, J J
Warburton, D
Lalley, P A
O'Brien, S J
Producer:
19810623
In:
Birth defects original article series
vol. 15
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130.
Segmental trisomy as a mouse model for Down syndrome.
[electronic resource]
by
Davisson, M T
Schmidt, C
Reeves, R H
Irving, N G
Akeson, E C
Harris, B S
Bronson, R T
Producer:
19940330
In:
Progress in clinical and biological research
vol. 384
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131.
RNA expression and chromosomal location of the mouse long-chain acyl-CoA dehydrogenase gene.
[electronic resource]
by
Hinsdale, M E
Farmer, S C
Johnson, K R
Davisson, M T
Hamm, D A
Tolwani, R J
Wood, P A
Producer:
19960201
In:
Genomics
vol. 28
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132.
Report of the committee on comparative mapping.
[electronic resource]
by
Lalley, P A
Davisson, M T
Graves, J A
O'Brien, S J
Roderick, T H
Doolittle, D P
Hillyard, A L
Producer:
19890209
In:
Cytogenetics and cell genetics
vol. 49
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133.
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.
[electronic resource]
by
Langner, C A
Birkenmeier, E H
Ben-Zeev, O
Schotz, M C
Sweet, H O
Davisson, M T
Gordon, J I
Producer:
19890630
In:
The Journal of biological chemistry
vol. 264
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134.
Grey intense: a new mouse mutation affecting pigmentation.
[electronic resource]
by
Davisson, M T
Johnson, K R
Bronson, R T
Ward-Bailey, P F
Cook, S A
Harris, B S
Donahue, L R
Producer:
20010222
In:
Mammalian genome : official journal of the International Mammalian Genome Society
vol. 11
Online resources:
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135.
Report of the Committee on Comparative Mapping.
[electronic resource]
by
Roderick, T H
Lalley, P A
Davisson, M T
O'Brien, S J
Womack, J E
Créau-Goldberg, N
Echard, G
Moore, K L
Producer:
19840214
In:
Cytogenetics and cell genetics
vol. 37
Online resources:
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136.
Mouse models of ocular diseases.
[electronic resource]
by
Chang, B
Hawes, N L
Hurd, R E
Wang, J
Howell, D
Davisson, M T
Roderick, T H
Nusinowitz, S
Heckenlively, J R
Producer:
20060120
In:
Visual neuroscience
vol. 22
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137.
Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract.
[electronic resource]
by
Smith, R S
Hawes, N L
Chang, B
Roderick, T H
Akeson, E C
Heckenlively, J R
Gong, X
Wang, X
Davisson, M T
Producer:
20000727
In:
Genomics
vol. 63
Online resources:
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138.
A mouse model for Down syndrome exhibits learning and behaviour deficits.
[electronic resource]
by
Reeves, R H
Irving, N G
Moran, T H
Wohn, A
Kitt, C
Sisodia, S S
Schmidt, C
Bronson, R T
Davisson, M T
Producer:
19951102
In:
Nature genetics
vol. 11
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139.
Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
[electronic resource]
by
Sundberg, J P
Boggess, D
Hogan, M E
Sundberg, B A
Rourk, M H
Harris, B
Johnson, K
Dunstan, R W
Davisson, M T
Producer:
19970731
In:
The American journal of pathology
vol. 151
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140.
Mouse chromosome fragility.
[electronic resource]
by
Sanz, M M
Jenkins, E C
Brown, W T
Davisson, M T
Kevin, M J
Roderick, T H
Silverman, W P
Wisniewski, H M
Producer:
19860404
In:
American journal of medical genetics
vol. 23
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