Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts

被引:0
作者
Giuliana Giannuzzi
Nicolas Chatron
Katrin Mannik
Chiara Auwerx
Sylvain Pradervand
Gilles Willemin
Kendra Hoekzema
Xander Nuttle
Jacqueline Chrast
Marie C. Sadler
Eleonora Porcu
Yann Herault
Bertrand Isidor
Brigitte Gilbert-Dussardier
Evan E. Eichler
Zoltan Kutalik
Alexandre Reymond
机构
[1] University of Lausanne,Center for Integrative Genomics
[2] University of Milan,Department of Biosciences
[3] Hospices Civils de Lyon,Service de génétique
[4] University of Lyon,Department of Computational Biology
[5] Université Claude Bernard Lyon 1,Center for Primary Care and Public Health
[6] CNRS UMR-5310,Department of Genome Sciences
[7] INSERM U-1217,Center for Genomic Medicine
[8] Institut NeuroMyoGène,Department of Neurology
[9] University of Lausanne,Howard Hughes Medical Institute
[10] University of Lausanne,Department of Genetic Medicine and Development
[11] Swiss Institute of Bioinformatics,Medical Genetics
[12] University of Washington,Department of Medical Sciences
[13] Massachusetts General Hospital,Department of Clinical and Biological Sciences
[14] Harvard Medical School,undefined
[15] Program in Medical and Population Genetics and Stanley Center for Psychiatric Research,undefined
[16] Broad Institute,undefined
[17] University of Strasbourg,undefined
[18] CNRS,undefined
[19] INSERM,undefined
[20] PHENOMIN-ICS,undefined
[21] Institute of Genetics and Molecular and Cellular Biology,undefined
[22] Service de Génétique Médicale,undefined
[23] CHU de Nantes,undefined
[24] Service de Génétique,undefined
[25] CHU de Poitiers,undefined
[26] University of Washington,undefined
[27] Centre Hospitalier Universitaire Vaudois,undefined
[28] University of Lausanne,undefined
[29] University of Montreal,undefined
[30] University of Geneva Medical School,undefined
[31] Service de Génétique Medicale,undefined
[32] CHU de Caen,undefined
[33] Service de Génétique Clinique,undefined
[34] CHU Paris-GH La Pitié Salpêtrière,undefined
[35] Service de Génétique Clinique,undefined
[36] CHU de Lille,undefined
[37] University of Siena,undefined
[38] University of Turin,undefined
[39] University of Turin,undefined
[40] Health 2030 Genome Center,undefined
[41] Foundation Campus Biotech,undefined
来源
npj Genomic Medicine | / 8卷
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[31]   Social behavior in 16p11.2 and 22q11.2 copy number variations: Insights from mice and humans [J].
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