Prognostic significance of chromosome 3 alterations determined by microsatellite analysis in uveal melanoma: a long-term follow-up study von Thomas, S, Pütter, C, Weber, S, Bornfeld, N, Lohmann, D R, Zeschnigk, M

Volltext

Spectrum of gross deletions and insertions in the RB1 gene in patients with retinoblastoma and association with phenotypic expression von Albrecht, P., Ansperger-Rescher, B., Schüler, A., Zeschnigk, M., Gallie, B., Lohmann, D.R.

Volltext

Age at diagnosis of isolated unilateral retinoblastoma does not distinguish patients with and without a constitutional RB1 gene mutation but is influenced by a parent-of-origin eff... von Schüler, A., Weber, S., Neuhäuser, M., Jurklies, C., Lehnert, T., Heimann, H., Rudolph, G., Jöckel, K.-H., Bornfeld, N., Lohmann, D.R.

Volltext

Constitutional RB1-Gene Mutations in Patients with Isolated Unilateral Retinoblastoma von Lohmann, Dietmar R., Gerick, Martin, Brandt, Birgit, Oelschläger, Ulrich, Lorenz, Birgit, Passarge, Eberhard, Horsthemke, Bernhard

Volltext

The spectrum of RB1 germ-line mutations in hereditary retinoblastoma von Lohmann, D R, Brandt, B, Höpping, W, Passarge, E, Horsthemke, B

Volltext

Marked differences in unilateral isolated retinoblastomas from young and older children studied by comparative genomic hybridization von HERZOG, Susanne, LOHMANN, Dietmar R, BUITING, Karin, SCHÜLER, Andreas, HORSTHEMKE, Bernhard, REHDER, Helga, RIEDER, Harald

Volltext

RB1 gene mutations in retinoblastoma von Lohmann, Dietmar R.

Volltext

Recurrent deletion of a region containing exon 24 of the RB1 gene caused by non-homologous recombination between a LINE-1HS and MER21B element von Albrecht, P, Bode, J, Buiting, K, Prashanth, A K, Lohmann, D R

Volltext

RB1 Gene Mutations in Peripheral Blood DNA of Patients with Isolated Unilateral Retinoblastoma von Klutz, Martina, Horsthemke, Bernhard, Lohmann, Dietmar R.

Volltext

Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma von LOHMANN, D. R, BRANDT, B, HÖPPING, W, PASSARGE, E, HORSTHEMKE, B

Volltext

First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome von Beygo, J., Buiting, K., Seland, S., Lüdecke, H.-J., Hehr, U., Lich, C., Prager, B., Lohmann, D.R., Wieczorek, D.

Volltext

Effects of Zinc and Cadmium on Apoptotic DNA Fragmentation in Isolated Bovine Liver Nuclei von Lohmann, Ruth D., Beyersmann, Detmar

Volltext

No association between the presence of a constitutional RB1 gene mutation and age in 68 patients with isolated unilateral retinoblastoma von Lohmann, D R, Horsthemke, B

Volltext

Effects of Zinc and Cadmium on Apoptotic DNA Fragmentation in Isolated Bovine Liver Nuclei von Lohmann, Ruth D., Beyersmann, Detmar

Volltext

Infrequent mutations of the p53 gene in pulmonary carcinoid tumors von LOHMANN, D. R, FESSELER, B, PÜTZ, B, REICH, U, BÖHM, J, PRÄUER, H, WÜNSCH, P. H, HÖFLER, H

Volltext

Partial deletions of the long and short arm of chromosome 3 point to two tumor suppressor genes in uveal melanoma von TSCHENTSCHER, Frank, PRESCHER, Gabriele, LOHMANN, Dietmar R, ZESCHNIGK, Michael, HORSMAN, Douglas E, WHITE, Valerie A, RIEDER, Harald, ANASTASSIOU, Gerasimos, SCHILLING, Harald, BORNFELD, Norbert, BARTZ-SCHMIDT, Karl Ulrich, HORSTHEMKE, Bernhard

Volltext

Multiple subcutaneous granular-cell tumours in a patient with Noonan syndrome von Lohmann, D R, Gillessen-Kaesbach, G

Volltext

Spectrum of small length germline mutations in the RB1 gene von Lohmann, Dletmar R., Brandt, Birglt, Höpping, Wolfgang, Passarge, Eberhard, Horsthemke, Bernhard

Volltext

Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastoma von Szijan, I, Lohmann, D R, Parma, D L, Brandt, B, Horsthemke, B

Volltext

Multiple lipomas linked to an RB1 gene mutation in a large pedigree with low penetrance retinoblastoma von Genuardi, M, Klutz, M, Devriendt, K, Caruso, D, Stirpe, M, Lohmann, D R

Volltext