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Chromosomal phenotypes and submicroscopic abnormalities
The finding, during the last decade, that several common, clinically delineated syndromes are caused by submicroscopic deletions or, more rarely, by duplications, has provided a powerful tool in the annotation of the human genome. Since most microdeletion/microduplication syndromes are defined by a...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2004
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525070/ https://www.ncbi.nlm.nih.gov/pubmed/15601540 http://dx.doi.org/10.1186/1479-7364-1-2-126 |