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Detailed Analysis of 22q11.2 With a High Density MLPA Probe Set
The presence of chromosome-specific low-copy repeats (LCRs) predisposes chromosome 22 to deletions and duplications. The current diagnostic procedure for detecting aberrations at 22q11.2 is chromosomal analysis coupled with fluorescence in situ hybridization (FISH) or PCR-based multiplex ligation de...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2664158/ https://ncbi.nlm.nih.gov/pubmed/18033723 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.20640 |
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