B. Schmalenberger

Cytogenetic survey of 32 cancers of the prostate.

H. Kastendieck, P. Carl, A. Rodewald, 1993, Cancer genetics and cytogenetics.

FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy

S. Balcı, F. Majewski, G. Hinkel, 1999, European Journal of Human Genetics.

Tuberous sclerosis in a child with de novo translocation t(3; 12) (p26.3; q23.3)

R. Fahsold, U. Claussen, H. Rott, 1991, Clinical genetics.

Screening of the 1 Mb SOX9 5′ control region by array CGH identifies a large deletion in a case of campomelic dysplasia with XY sex reversal

K. Lindenberg, S. Blesson, G. Scherer, 2004, Journal of Medical Genetics.

Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene

M. Rietschel, G. Danieli, K. Zerres, 1992, Neuromuscular Disorders.

The fragile-X phenotype. Computer assisted analysis of the dysmorphological features and discrimination from the Sotos phenotype.

R. Fahsold, B. Schmalenberger, S. Stengel-Rutkowski, 1993, Genetic counseling.

A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly.

U. Müller, D. Steinberger, H. Collmann, 1997, Journal of medical genetics.