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De novo 13q31.1–q32.1 interstitial deletion encompassing the miR‐17‐92 cluster in a patient with Feingold syndrome‐2 |
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| Authors: | E. Tassano Ph.D. M. Di Rocco S. Signa G. Gimelli |
| Affiliation: | 1. Laboratorio di Citogenetica, Istituto G. Gaslini, Genova, Italy;2. Unit of Rare Diseases, Department of Pediatrics, Istituto G. Gaslini, Genova, Italy |
| Abstract: | |
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