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A Deficiency in the Region Homologous to Human 17q21.33–q23.2 Causes Heart Defects in Mice
Several constitutional chromosomal rearrangements occur on human chromosome 17. Patients who carry constitutional deletions of 17q21.3–q24 exhibit distinct phenotypic features. Within the deletion interval, there is a genomic segment that is bounded by the myeloperoxidase and homeobox B1 genes. This...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Copyright © 2006 by the Genetics Society of America
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1461454/ https://ncbi.nlm.nih.gov/pubmed/16489219 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.105.054833 |
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