A long range restriction map of the pseudoautosomal region by partial digest PFGE analysis from the telomere.

por Rappold, G A, Lehrach, H
Publicado 1988

Identification of a testis-specific gene from the mouse t-complex next to a CpG-rich island.

por Rappold, G A, Stubbs, L, Labeit, S, Crkvenjakov, R B, Lehrach, H
Publicado 1987

Rare SHANK2 variants in schizophrenia

por Peykov, S, Berkel, S, Degenhardt, F, Rietschel, M, Nöthen, M M, Rappold, G A
Publicado en Mol Psychiatry (2015)

Pseudoautosomal marker DXYS20 and manic depression.

por Nöthen, M M, Cichon, S, Erdmann, J, Körner, J, Rietschel, M, Rappold, G A, Fritze, J, Propping, P
Publicado 1993

c-myc and immunoglobulin kappa light chain constant genes are on the 8q+ chromosome of three Burkitt lymphoma lines with t(2;8) translocations.

por Rappold, G A, Hameister, H, Cremer, T, Adolph, S, Henglein, B, Freese, U K, Lenoire, G M, Bornkamm, G W
Publicado 1984

Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour

por Bacon, C, Schneider, M, Le Magueresse, C, Froehlich, H, Sticht, C, Gluch, C, Monyer, H, Rappold, G A
Publicado en Mol Psychiatry (2015)

5q31 Microdeletions: Definition of a Critical Region and Analysis of LRRTM2, a Candidate Gene for Intellectual Disability

por Kleffmann, W., Zink, A.M., Lee, J.A., Senderek, J., Mangold, E., Moog, U., Rappold, G.A., Wohlleber, E., Engels, H.
Publicado 2012

Identification and functional characterization of rare SHANK2 variants in schizophrenia

por Peykov, S, Berkel, S, Schoen, M, Weiss, K, Degenhardt, F, Strohmaier, J, Weiss, B, Proepper, C, Schratt, G, Nöthen, M M, Boeckers, T M, Rietschel, M, Rappold, G A
Publicado en Mol Psychiatry (2015)