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SNP array mapping of 20p deletions: Genotypes, Phenotypes and Copy Number Variation
The use of array technology to define chromosome deletions and duplications is bringing us closer to establishing a genotype/phenotype map of genomic copy number alterations. We studied 21 patients and 5 relatives with deletions of the short arm of chromosome 20 using the Illumina HumanHap550 SNP ar...
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| Main Authors: | , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2009
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2650004/ https://ncbi.nlm.nih.gov/pubmed/19058200 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.20863 |
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