Abstract. Mice that are homozygous for the autosomal recessive hydrocephaly with hop gait (hyh) mutation on Chromosome (Chr) 7 have congenital hydrocephalus characterized by an interhemi-spheric cyst arising from the third ventricle and agenesis of the corpus callosum. Analysis of more than 500 backcross and inter-cross progeny maps the hyh locus to proximal Chr 7, approxi-mately 13 cM centromeric to its originally reported map position. Analysis of recombinants at several MIT microsatellite markers localized the hyh locus between D7Mit75 and D7Mit56. Develop-ment of several new SSLP markers allowed us to refine the hyh candidate interval to a region defined by the cone-rod homeobox (Crx) gene proximally and D7Mit56 distally. A contig of ye...
Motor neuron disease is a progressive genetic disorder with 5 sufferers per 100,000 people in Europe...
Myelencephalic blebs (my) is a recessively inherited mutation on mouse Chr 3. Embryonic subepidermal...
The hedgehog genes encode signaling molecules that play a role in regulating embryonic morphogenesis...
Mice that are homozygous for the autosomal recessive hydrocephaly with hop gait (hyh) mutation on Ch...
Mutations in the mouse dreher (dr) gene cause skeletal defects, hyperactivity, abnormal gait, deafne...
An 8-Mb yeast artificial chromosome (YAC) contig has been constructed spanning 9 cM on mouse proxima...
The Ames dwarf is a mouse mutant characterized by a reduced body size and infertility caused by lack...
Functional characterization of the mouse genome requires the availability of a comprehensive physica...
This paper uses cytotoxic and proliferative T cell clones specific for H-Y and restricted by MHC mol...
We identified a semidominant, chemically induced, mouse use mutation with a complex array of abnorma...
The mouse Ulnaless locus is a semidominant mutation which displays defects in patterning along the p...
The locus of the structural gene encoding tyrosine hydroxylase, Th, the rate limiting enzyme for cat...
Huntington's disease (HD) is a devastating central nervous system disorder. Even though the gene res...
A physical map of the mouse genome is an essential tool for both positional cloning and genomic sequ...
Mouse mutants provide an opportunity to clone novel genes that are involved in specific biological p...
Motor neuron disease is a progressive genetic disorder with 5 sufferers per 100,000 people in Europe...
Myelencephalic blebs (my) is a recessively inherited mutation on mouse Chr 3. Embryonic subepidermal...
The hedgehog genes encode signaling molecules that play a role in regulating embryonic morphogenesis...
Mice that are homozygous for the autosomal recessive hydrocephaly with hop gait (hyh) mutation on Ch...
Mutations in the mouse dreher (dr) gene cause skeletal defects, hyperactivity, abnormal gait, deafne...
An 8-Mb yeast artificial chromosome (YAC) contig has been constructed spanning 9 cM on mouse proxima...
The Ames dwarf is a mouse mutant characterized by a reduced body size and infertility caused by lack...
Functional characterization of the mouse genome requires the availability of a comprehensive physica...
This paper uses cytotoxic and proliferative T cell clones specific for H-Y and restricted by MHC mol...
We identified a semidominant, chemically induced, mouse use mutation with a complex array of abnorma...
The mouse Ulnaless locus is a semidominant mutation which displays defects in patterning along the p...
The locus of the structural gene encoding tyrosine hydroxylase, Th, the rate limiting enzyme for cat...
Huntington's disease (HD) is a devastating central nervous system disorder. Even though the gene res...
A physical map of the mouse genome is an essential tool for both positional cloning and genomic sequ...
Mouse mutants provide an opportunity to clone novel genes that are involved in specific biological p...
Motor neuron disease is a progressive genetic disorder with 5 sufferers per 100,000 people in Europe...
Myelencephalic blebs (my) is a recessively inherited mutation on mouse Chr 3. Embryonic subepidermal...
The hedgehog genes encode signaling molecules that play a role in regulating embryonic morphogenesis...