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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...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2004
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3525070/ https://ncbi.nlm.nih.gov/pubmed/15601540 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-7364-1-2-126 |
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