Published in Genome Res on November 01, 1997
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Hair interior defect in AKR/J mice. Clin Exp Dermatol (2009) 0.99
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Localization of a murine recessive polycystic kidney disease mutation and modifying loci that affect disease severity. Genomics (1995) 0.98
Identification and genetic mapping of a new polycystic kidney disease on mouse chromosome 8. Genomics (1997) 0.98
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Quantitative trait locus mapping of airway responsiveness to chromosomes 6 and 7 in inbred mice. Am J Physiol (1999) 0.95
A novel putative transporter maps to the osteosclerosis (oc) mutation and is not expressed in the oc mutant mouse. Genomics (1999) 0.95
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Structure and mapping of the mouse matrilin-3 gene (Matn3), a member of a gene family containing a U12-type AT-AC intron. Mamm Genome (2000) 0.89
An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1). Genomics (1997) 0.88
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Spx1, a novel X-linked homeobox gene expressed during spermatogenesis. Mech Dev (1997) 0.84
Genetic analysis of modifying loci on mouse chromosome 1 that affect disease severity in a model of recessive PKD. Physiol Genomics (1999) 0.84
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CD19 maps to a region of conservation between human chromosome 16 and mouse chromosome 7. Immunogenetics (1994) 0.84
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