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Molecular Vision
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November 4, 2000
Further genetic analysis of two autosomal dominant mouse eye defects, Ccw and Pax6(coop)
M F Lyon, D Bogani, Y Boyd, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 1, 1994
Mapping of loci and translocation breakpoints in Xq13: isolation of a conserved locus that maps close to CCG1 in human and mouse
V Reed, S H Laval, V McCabe, et al.
Genome Research
|
March 18, 2000
A phenotype map of the mouse X chromosome: models for human X-linked disease
Y Boyd, H J Blair, P Cunliffe, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1994
Mouse X chromosome
G E Herman, Y Boyd, V Chapman, et al.
Genomics
|
August 10, 1995
Mapping of the mouse homologue of the Wilson disease gene to mouse chromosome 8
V Reed, P Williamson, P C Bull, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Factors affecting the expression of genes on chromosome 9
S Povey, Y Boyd, M E Duncan, et al.
Scandinavian Journal of Immunology
|
July 6, 2001
Structure and chromosomal localization of chicken CD5
R Koskinen, J Salomonsen, M Goodchild, et al.
Development (Cambridge, England)
|
July 22, 1998
Evidence that preaxial polydactyly in the Doublefoot mutant is due to ectopic Indian Hedgehog signaling
Y Yang, P Guillot, Y Boyd, et al.
Journal of Medical Genetics
|
December 1, 1986
Muscular dystrophy in girls with X;autosome translocations
Y Boyd, V Buckle, S Holt, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 1, 1994
Evaluation of human microdissection clones from the FRAXA region as tools for comparative mapping in the mouse: isolation of a conserved genomic clone close to FMR1
H J Blair, M C Hirst, R MacKinnon, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 95) with videos related to
Sort By:
Page
of 10
Molecular Vision
|
November 4, 2000
Further genetic analysis of two autosomal dominant mouse eye defects, Ccw and Pax6(coop)
M F Lyon, D Bogani, Y Boyd, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
April 1, 1994
Mapping of loci and translocation breakpoints in Xq13: isolation of a conserved locus that maps close to CCG1 in human and mouse
V Reed, S H Laval, V McCabe, et al.
Genome Research
|
March 18, 2000
A phenotype map of the mouse X chromosome: models for human X-linked disease
Y Boyd, H J Blair, P Cunliffe, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1994
Mouse X chromosome
G E Herman, Y Boyd, V Chapman, et al.
Genomics
|
August 10, 1995
Mapping of the mouse homologue of the Wilson disease gene to mouse chromosome 8
V Reed, P Williamson, P C Bull, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Factors affecting the expression of genes on chromosome 9
S Povey, Y Boyd, M E Duncan, et al.
Scandinavian Journal of Immunology
|
July 6, 2001
Structure and chromosomal localization of chicken CD5
R Koskinen, J Salomonsen, M Goodchild, et al.
Development (Cambridge, England)
|
July 22, 1998
Evidence that preaxial polydactyly in the Doublefoot mutant is due to ectopic Indian Hedgehog signaling
Y Yang, P Guillot, Y Boyd, et al.
Journal of Medical Genetics
|
December 1, 1986
Muscular dystrophy in girls with X;autosome translocations
Y Boyd, V Buckle, S Holt, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 1, 1994
Evaluation of human microdissection clones from the FRAXA region as tools for comparative mapping in the mouse: isolation of a conserved genomic clone close to FMR1
H J Blair, M C Hirst, R MacKinnon, et al.
Page
of 10