Exclusion of a disease relevant role of PAX4 in the aetiology of Silver-Russell syndrome: screening for mutations and determination of imprinting status

gan MERGENTHALER, S., EGGERMANN, K., TOMIUK, J., RANKE, M., WOLLMANN, H., EGGERMANN, T.
Cyhoeddwyd 2000

Uniparental isodisomy for paternal 2p and maternal 2q in a phenotypically normal female with two isochromosomes, i(2p) and i(2q)

gan ALBRECHT, B., MERGENTHALER, S., EGGERMANN, K., ZERRES, K., PASSARGE, E., EGGERMANN, T.
Cyhoeddwyd 2001

Paternally inherited deletion of CSH1 in a patient with Silver-Russell syndrome.

gan Eggermann, T, Eggermann, K, Mergenthaler, S, Kuner, R, Kaiser, P, Ranke, M B, Wollmann, H A
Cyhoeddwyd 1998

Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients

gan Eggermann, T., Mergenthaler, S., Eggermann, K., Albers, A., Linnemann, K., Fusch, C., Ranke, M., Wollmann, H.
Cyhoeddwyd 2001

Is maternal duplication of 11p15 associated with Silver-Russell syndrome?

gan Eggermann, T, Meyer, E, Obermann, C, Heil, I, Schuler, H, Ranke, M, Eggermann, K, Wollmann, H
Cyhoeddwyd 2005

Epigenetic mutations in 11p15 in Silver‐Russell syndrome are restricted to the telomeric imprinting domain

gan Eggermann, T, Schönherr, N, Meyer, E, Obermann, C, Mavany, M, Eggermann, K, Ranke, M B, Wollmann, H A
Cyhoeddwyd 2006

Association analysis of the monoamine oxidase A gene in bipolar affective disorder by using family-based internal controls.

gan Nöthen, M M, Eggermann, K, Albus, M, Borrmann, M, Rietschel, M, Körner, J, Maier, W, Minges, J, Lichtermann, D, Franzek, E
Cyhoeddwyd 1995

Nonreplication of linkage disequilibrium between the dopamine D4 receptor locus and Tourette syndrome.

gan Hebebrand, J, Nöthen, M M, Ziegler, A, Klug, B, Neidt, H, Eggermann, K, Lehmkuhl, G, Poustka, F, Schmidt, M H, Propping, P, Remschmidt, H
Cyhoeddwyd 1997