Search Results - Mathey, C. M.
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Contribution of rare and potentially functionally relevant sequence variants in schizophrenia risk-Locus Xq28,distal by Claus, Isabelle (Author) , Sivalingam, S. (Author) , Koller, A. C. (Author) , Weiß, A. (Author) , Mathey, C. M. (Author) , Sindermann, L. (Author) , Klein, D. (Author) , Henschel, L. (Author) , Ludwig, K. U. (Author) , Hoffmann, P. (Author) , Heimbach, A. (Author) , Heilmann-Heimbach, S. (Author) , Vedder, H. (Author) , Kammerer-Ciernioch, J. (Author) , Stürmer, T. (Author) , Streit, Fabian (Author) , Maaser-Hecker, A. (Author) , Nenadić, I. (Author) , Baune, B. T. (Author) , Hartmann, A. M. (Author) , Konte, B. (Author) , Giegling, I. (Author) , Heilbronner, U. (Author) , Wagner, M. (Author) , Philipsen, A. (Author) , Schmidt, B. (Author) , Rujescu, D. (Author) , Buness, A. (Author) , Schulze, T. G. (Author) , Rietschel, Marcella (Author) , Forstner, A. J. (Author) , Nöthen, M. M. (Author) , Degenhardt, F. (Author) ,
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Adult
Case-Control Studies
Chromosomes, Human, X
Cohort Studies
European People
Female
Genetic Loci
Genetic Predisposition to Disease
Genetic Variation
Germany
Humans
Male
Polymorphism, Single Nucleotide
Risk Factors
Schizophrenia
X‐chromosome
burden analysis
copy number variation
rare variants
schizophrenia