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A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility

C Fernandez-Rozadilla1, J B Cazier, I Tomlinson

  • 1Fundación Pública Galega de Medicina Xenómica (FPGMX)-SERGAS, Grupo de Medicina Xenómica, IDIS, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERer), Complexo Hospitalario Universitario de Santiago, Choupana s/n, 15706, Santiago, Spain.

Human Genetics
|November 13, 2013
PubMed

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