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Copy number variations in 119 Chinese children with idiopathic short stature identified by the custom genome-wide microarray
BACKGROUND: Idiopathic short stature (ISS) refers to short stature with no evident etiologies. The custom genome-wide microarray specifically designed to cover height-related genes may be helpful to detect copy number variations (CNVs) in ISS patients, which may be missed by the general microarray....
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| Udgivet i: | Mol Cytogenet |
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| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2016
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4755006/ https://ncbi.nlm.nih.gov/pubmed/26884814 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-016-0225-0 |
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