Fortuitous detection of a submicroscopic deletion at 1q25 in a girl with Cornelia-de Lange syndrome carrying t(5;13)(p13.1;q12.1) by array-based comparative genomic hybridization.
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| Description | scientific article published in June 2007 |
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author: Issei Imoto Shin Hayashi |
| Publication date | June 1, 2007 |
| Language | English |
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