| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5589021 | European Journal of Medical Genetics | 2017 | 4 Pages |
Abstract
We identified by microarray analysis a new case of 12q15 deletion. Our patient clinical features allow the refinement of the SRO to CNOT2, KCNMB4, and PTPRB genes, improving genotype-phenotype correlations.
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Authors
Viola Alesi, Sara Loddo, Marta Grispo, Simona Riccio, Andrea Costantino Montella, Bruno Dallapiccola, Lucia Ulgheri, Antonio Novelli,