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Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits
We describe two patients carrying deletions of chromosome 8p23.1 with a commonly critical region identified by means of oligonucleotide array comparative genomic hybridization (array CGH). They didn't present congenital heart defects or behavioral problems. Only one patient presented with intel...
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| Pubblicato in: | J Pediatr Genet |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Georg Thieme Verlag KG
2015
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| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4906530/ https://ncbi.nlm.nih.gov/pubmed/27617130 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0035-1565269 |
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