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A novel description of a syndrome consisting of 7q21.3 deletion including DYNC1I1 with preserved DLX5/6 without ectrodactyly: a case report
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| Título de la Revista: | JOURNAL OF MEDICAL CASE REPORTS |
| Volumen: | 10 |
| Número: | 1 |
| Fecha de publicación: | 2016 |
| URL: | 10.1186/s13256-016-0921-8 |
| DOI: |
10.1186/s13256-016-0921-8 |