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

Por MERGENTHALER, S., EGGERMANN, K., TOMIUK, J., RANKE, M., WOLLMANN, H., EGGERMANN, T.
Publicado em 2000

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

Por ALBRECHT, B., MERGENTHALER, S., EGGERMANN, K., ZERRES, K., PASSARGE, E., EGGERMANN, T.
Publicado em 2001

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

Por Eggermann, T, Eggermann, K, Mergenthaler, S, Kuner, R, Kaiser, P, Ranke, M B, Wollmann, H A
Publicado em 1998

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

Por Eggermann, T., Mergenthaler, S., Eggermann, K., Albers, A., Linnemann, K., Fusch, C., Ranke, M., Wollmann, H.
Publicado em 2001

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

Por Eggermann, T, Meyer, E, Obermann, C, Heil, I, Schuler, H, Ranke, M, Eggermann, K, Wollmann, H
Publicado em 2005

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

Por Eggermann, T, Schönherr, N, Meyer, E, Obermann, C, Mavany, M, Eggermann, K, Ranke, M B, Wollmann, H A
Publicado em 2006

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

Por Nöthen, M M, Eggermann, K, Albus, M, Borrmann, M, Rietschel, M, Körner, J, Maier, W, Minges, J, Lichtermann, D, Franzek, E
Publicado em 1995

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

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