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

par MERGENTHALER, S., EGGERMANN, K., TOMIUK, J., RANKE, M., WOLLMANN, H., EGGERMANN, T.
Publié 2000

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

par ALBRECHT, B., MERGENTHALER, S., EGGERMANN, K., ZERRES, K., PASSARGE, E., EGGERMANN, T.
Publié 2001

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

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

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

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

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

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

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

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

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

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

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

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