Sequencing of a patient with balanced chromosome abnormalities and neurodevelopmental disease identifies disruption of multiple high risk loci by structural variation (Q35119909)
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English | Sequencing of a patient with balanced chromosome abnormalities and neurodevelopmental disease identifies disruption of multiple high risk loci by structural variation |
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Sequencing of a patient with balanced chromosome abnormalities and neurodevelopmental disease identifies disruption of multiple high risk loci by structural variation (English)
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Ute Moog
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Jonathon Blake
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Andrew Riddell
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Susanne Theiss
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Anna Jauch
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Johannes W G Janssen
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David Ibberson
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Dinko Pavlinic
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Heiko Runz
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13 March 2014
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e90894
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13 March 2014
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