Somatic mosaicism in a patient with bilateral retinoblastoma.

Autor Greger, V, Passarge, E, Horsthemke, B
Vydáno 1990

A simple and nonradioactive method for detecting the Rb1.20 DNA polymorphism in the retinoblastoma gene.

Autor Brandt, B, Greger, V, Yandell, D, Passarge, E, Horsthemke, B
Vydáno 1992

Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma.

Autor Greger, V, Kerst, S, Messmer, E, Höpping, W, Passarge, E, Horsthemke, B
Vydáno 1988

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.

Autor Reis, A., Dittrich, B., Greger, V., Buiting, K., Lalande, M., Gillessen-Kaesbach, G., Anvret, M., Horsthemke, B.
Vydáno 1994

A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes.

Autor Buiting, K, Greger, V, Brownstein, B H, Mohr, R M, Voiculescu, I, Winterpacht, A, Zabel, B, Horsthemke, B
Vydáno 1992

Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.

Autor Greger, V, Knoll, J H, Wagstaff, J, Woolf, E, Lieske, P, Glatt, H, Benn, P A, Rosengren, S S, Lalande, M
Vydáno 1997