PuSH - Publication Server of Helmholtz Zentrum München

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1.
Jansen, I.E.* et al.: Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing. Genome Biol. 18:22 (2017)
2.
Reijnders, M.R.* et al.: PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature. J. Med. Genet. 55, 104-113 (2017)
3.
Mok, K.Y.* et al.: Deletions at 22q11.2 in idiopathic Parkinson's disease: A combined analysis of genome-wide association data. Lancet Neurol. 15, 585-596 (2016)