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Author Report for: Ropers HH

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    Title: Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree
    Lesch KP, Selch S, Renner TJ, Jacob C, Nguyen TT, Hahn T, Romanos M, Walitza S, Shoichet S and Ullmann R <15 more author(s)>
    Ref: Mol Psychiatry, 16:491, 2011 : PubMed

            

    Title: X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
    Laumonnier F, Bonnet-Brilhault F, Gomot M, Blanc R, David A, Moizard MP, Raynaud M, Ronce N, Lemonnier E and Briault S <9 more author(s)>
    Ref: American Journal of Human Genetics, 74:552, 2004 : PubMed

            

    Title: Molecular cloning and characterization of the Fugu rubripes MEST/COPG2 imprinting cluster and chromosomal localization in Fugu and Tetraodon nigroviridis
    Brunner B, Grutzner F, Yaspo ML, Ropers HH, Haaf T, Kalscheuer VM
    Ref: Chromosome Res, 8:465, 2000 : PubMed

            

    Title: Evidence against a major role of PEG1/MEST in Silver-Russell syndrome
    Riesewijk AM, Blagitko N, Schinzel AA, Hu L, Schulz U, Hamel BC, Ropers HH, Kalscheuer VM
    Ref: Eur J Hum Genet, 6:114, 1998 : PubMed

            

    Title: Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses
    Riesewijk AM, Hu L, Schulz U, Tariverdian G, Hoglund P, Kere J, Ropers HH, Kalscheuer VM
    Ref: Genomics, 42:236, 1997 : PubMed

            


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