1996
DOI: 10.1093/genetics/143.1.447
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Complementation Mapping of Skeletal and Central Nervous System Abnormalities in Mice of the piebald Deletion Complex

Abstract: The s15DttMb, s36Pub, s1Acrg and s24Pub piebald deletion alleles belong to a set of overlapping deficiencies on the distal portion of chromosome 14. Molecular analysis was used to define the extent of the deletions. Mice homozygous for the smallest deletion, s15DttMb, die shortly after delivery and display alterations in the central nervous system, including hydrocephalus and a dorsally restricted malformation of the spinal cord. These mice also display homeotic transformations of vertebrae in the midthoracic … Show more

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Cited by 31 publications
(1 citation statement)
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“…The piebald deletion mouse model is a collection of overlapping Mb-scale chromosomal deletions centred around the endothelia receptor B (Ednrb) coat colour spotting locus (O'Brien et al, 1996). In a previous study, we have used these mouse models to annotate the function of a distal 6Mb region of mouse chromosome 14.…”
Section: Resultsmentioning
confidence: 99%
“…The piebald deletion mouse model is a collection of overlapping Mb-scale chromosomal deletions centred around the endothelia receptor B (Ednrb) coat colour spotting locus (O'Brien et al, 1996). In a previous study, we have used these mouse models to annotate the function of a distal 6Mb region of mouse chromosome 14.…”
Section: Resultsmentioning
confidence: 99%