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Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletion
BACKGROUND: Interstitial 6q deletions, involving the 6q15q25 chromosomal region, are rare events characterized by variable phenotypes and no clear karyotype/phenotype correlation has been determined yet. RESULTS: We present a child with a 6q21q22.1 deletion, characterized by array-CGH, associated wi...
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| 出版年: | Mol Cytogenet |
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| 主要な著者: | , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4457201/ https://ncbi.nlm.nih.gov/pubmed/26052347 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-015-0134-7 |
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