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Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication
BACKGROUND: Little information is available regarding the penetrance of 1q21.1 copy number variants (CNVs). In the present study, we explored the clinical significance of 1q21.1 microdeletion or microduplication. METHODS: In four families, chromosome karyotype was analyzed using G‐banding karyotype...
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| 出版年: | J Gene Med |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5413856/ https://ncbi.nlm.nih.gov/pubmed/28220983 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jgm.2948 |
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