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Genotype–Phenotype Association Studies of Chromosome 8p Inverted Duplication Deletion Syndrome
Individuals diagnosed with chromosome 8p inverted duplication deletion (invdupdel(8p)) manifest a wide range of clinical features and cognitive impairment. The purpose of this study is to employ array CGH technology to define more precisely the cytogenetic breakpoints and regions of copy number vari...
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| Pubblicato in: | Behav Genet |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2011
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4557779/ https://ncbi.nlm.nih.gov/pubmed/21259039 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10519-011-9447-4 |
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