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Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome
Williams-Beuren syndrome (WBS) is a neurological disorder resulting from a microdeletion, typically 1.5 megabases in size, at 7q11.23. Atypical patients implicate genes at the telomeric end of this multigene deletion as the main candidates for the pathology of WBS in particular the unequal cognitive...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Cold Spring Harbor Laboratory Press
2004
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2286546/ https://ncbi.nlm.nih.gov/pubmed/15388857 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1110/ps.04747604 |
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