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Rare Copy Number Variants Are a Common Cause of Short Stature
Human growth has an estimated heritability of about 80%–90%. Nevertheless, the underlying cause of shortness of stature remains unknown in the majority of individuals. Genome-wide association studies (GWAS) showed that both common single nucleotide polymorphisms and copy number variants (CNVs) contr...
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| Main Authors: | , , , , , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Public Library of Science
2013
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3597495/ https://ncbi.nlm.nih.gov/pubmed/23516380 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1003365 |
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