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Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2
BACKGROUND: We report on a young female, who presents with a severe speech and language disorder and a balanced de novo complex chromosomal rearrangement, likely to have resulted from a chromosome 7 pericentromeric inversion, followed by a chromosome 7 and 11 translocation. RESULTS: Using molecular...
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| Pubblicato in: | Mol Cytogenet |
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| Autori principali: | , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4460787/ https://ncbi.nlm.nih.gov/pubmed/26060509 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-015-0148-1 |
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