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L. L. Field et al.
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Katannya Kapeli et al.
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Rami Abou Jamra et al.
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Pia Villanueva et al.
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Holly E. Ainsworth et al.
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D. V. M. Bishop et al.
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J. Elia et al.
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Ivan A. Adzhubei et al.
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Data quality control in genetic case-control association studies
Carl A. Anderson et al.
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Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13
Stormy J. Chamberlain et al.
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Delphine Fradin et al.
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Dianne F. Newbury et al.
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J. Yan et al.
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Takuro Horii et al.
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Maricela Alarcon et al.
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Shaun Purcell et al.
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SE Newey et al.
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E Viding et al.
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YH Wang et al.
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J Tzenova et al.
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