B. Weber

发表

Studies of the RB1 gene and the p53 gene in human osteosarcomas.

G. Delling, H. Kabisch, K. Winkler, 1992, Pediatric hematology and oncology.

Methylation Status of the Retinoblastoma Gene (RB1) in Osteosarcoma: No Evidence for Hypermethylation

C. Otte, G. Delling, H. Kabisch, 2004 .

METHYLATION STATUS OF THE RETINOBLASTOMA GENE (RB1) IN OSTEOSARCOMA: No Evidence for Hypermethylation

C. Otte, G. Delling, H. Kabisch, 2004, Pediatric hematology and oncology.

A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype.

R. Schneppenheim, U. zur Stadt, H. Kabisch, 2004, Blood.

Polymorphisms of surfactant protein A genes and the risk of bronchopulmonary dysplasia in preterm infants.

A. Borkhardt, L. Gortner, I. Reiss, 2000, The Turkish journal of pediatrics.

Novel and recurrent mutations in the tyrosinase gene and the P gene in the German albino population

B. Weber, L. Passmore, B. Kaesmann-Kellner, 1999, Human Genetics.

High Positive Predictive Value (PPV) of Cell-Free DNA (cfDNA) Testing in a Clinical Study of 10,000 Consecutive Pregnancies

Čulić, R. Rijnders, M. Badura-Stronka, 2016 .

Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function

J. Fischer, C. Has, A. Vahlquist, 2017, The British journal of dermatology.

SV40 sequences in human osteosarcoma of German origin.

S. Bielack, G. Delling, P. Setlak, 2000, Anticancer research.