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

di Rappold, G A, Lehrach, H
Pubblicazione 1988

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

di Rappold, G A, Stubbs, L, Labeit, S, Crkvenjakov, R B, Lehrach, H
Pubblicazione 1987

Rare SHANK2 variants in schizophrenia

di Peykov, S, Berkel, S, Degenhardt, F, Rietschel, M, Nöthen, M M, Rappold, G A
Pubblicato in Mol Psychiatry (2015)

Pseudoautosomal marker DXYS20 and manic depression.

di Nöthen, M M, Cichon, S, Erdmann, J, Körner, J, Rietschel, M, Rappold, G A, Fritze, J, Propping, P
Pubblicazione 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.

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

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

di Bacon, C, Schneider, M, Le Magueresse, C, Froehlich, H, Sticht, C, Gluch, C, Monyer, H, Rappold, G A
Pubblicato in Mol Psychiatry (2015)

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

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

Identification and functional characterization of rare SHANK2 variants in schizophrenia

di 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
Pubblicato in Mol Psychiatry (2015)