Concomitant deletion of chromosome 16p13.11 and triplication of chromosome 19p13.3 in a child with developmental disorders, intellectual disability, and epilepsy.
Autor: | Tassano, Elisa1 eli.tassano@gmail.com, De Santis, Lucia Rosaia2, Corona, Maria Franca3, Parmigiani, Stefano4, Zanetti, Dalila2, Porta, Simona1, Gimelli, Giorgio1, Cuoco, Cristina1 |
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Zdroj: | Molecular Cytogenetics (17558166). 2015, Vol. 8 Issue 1, p1-5. 5p. |
Databáze: | Academic Search Ultimate |
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