Deletion of the App-Runx1 region in mice models human partial monosomy 21
Deletion of the App-Runx1 region in mice models human partial monosomy 21
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Publisher
England: The Company of Biologists Ltd
Journal title
Language
English
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Publisher
England: The Company of Biologists Ltd
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Partial monosomy 21 (PM21) is a rare chromosomal abnormality that is characterized by the loss of a variable segment along human chromosome 21 (Hsa21). The clinical phenotypes of this loss are heterogeneous and range from mild alterations to lethal consequences, depending on the affected region of Hsa21. The most common features include intellectua...
Alternative Titles
Full title
Deletion of the App-Runx1 region in mice models human partial monosomy 21
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TN_cdi_doaj_primary_oai_doaj_org_article_0c555f6364e54f5bb3de522f49323af9
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_0c555f6364e54f5bb3de522f49323af9
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ISSN
1754-8403,1754-8411
E-ISSN
1754-8411,1754-8403
DOI
10.1242/dmm.017814
