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Characterization of a Cryptic 3.3 Mb Deletion in a Patient With a “Balanced t(15;22) Translocation” Using High Density Oligo Array CGH and Gene Expression Arrays
Patients with an apparently balanced translocation and an abnormal phenotype may carry a cryptic deletion/duplication at their translocation breakpoints that may explain their abnormalities. Using microarray CGH (aCGH) and gene expression arrays we studied a child with t(15;22)(q26.1;q11.2), develop...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2008
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2810975/ https://ncbi.nlm.nih.gov/pubmed/18203177 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.32116 |
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