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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.
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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  Data: KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome.
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  Data: <searchLink fieldCode="JN" term="%22BMC+Medical+Genetics%22">BMC Medical Genetics</searchLink>. Aug2015, Vol. 16 Issue 1, p1-8. 8p.
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        Value: 10.1186/s12881-015-0211-0
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      – TitleFull: KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome.
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