Refinement of the deletion in 7q21.3 associated with split hand/foot malformation type 1 and Mondini dysplasia

Por Wieland, I, Muschke, P, Jakubiczka, S, Volleth, M, Freigang, B, Wieacker, P
Publicado em 2004

Partial trisomy 9p12p21.3 with a normal phenotype

Por Stumm, M, Musebeck, J, Tonnies, H, Volleth, M, Lemke, J, Chudoba, I, Wieacker, P
Publicado em 2002

Two further cases of WHS with unbalanced de novo translocation t(4;8) characterised by CGH and FISH

Por Tonnies, H., Stumm, M., Neumann, L., Volleth, M., Grumpelt, U., Musebeck, J., Annuss, G., Neitzel, H.
Publicado em 2001

Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes

Por Weise, A, Starke, H, Heller, A, Tonnies, H, Volleth, M, Stumm, M, Gabriele, S, Nietzel, A, Claussen, U, Liehr, T
Publicado em 2002

Human Ring Chromosomes – New Insights for their Clinical Significance

Por Guilherme, RS, Klein, E, Hamid, AB, Bhatt, S, Volleth, M, Polityko, A, Kulpanovich, A, Dufke, A, Albrecht, B, Morlot, S, Brecevic, L, Petersen, MB, Manolakos, E, Kosyakova, N, Liehr, T
Publicado em 201