KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome.
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| Title: | KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome. |
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| Authors: | Moreno-Igoa, María1, Hernández-Charro, Blanca1, Bengoa-Alonso, Amaya1, Pérez-Juana-del-Casal, Aranzazu1, Romero-Ibarra, Carlos2, Nieva-Echebarria, Beatriz3, Ramos-Arroyo, María Antonia1 ma.ramos.arroyo@navarra.es |
| Source: | BMC Medical Genetics. Aug2015, Vol. 16 Issue 1, p1-8. 8p. |
| Database: | Academic Search Ultimate |
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