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Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
BACKGROUND: Duplications and deletions in the human genome can cause disease or predispose persons to disease. Advances in technologies to detect these changes allow for the routine identification of submicroscopic imbalances in large numbers of patients. METHODS: We tested for the presence of micro...
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主要な著者: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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フォーマット: | Artigo |
言語: | Inglês |
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2008
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オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2703742/ https://ncbi.nlm.nih.gov/pubmed/18784092 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1056/NEJMoa0805384 |
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