C. Gadomski

发表

Isolation and characterization of a candidate gene for progressive myoclonus epilepsy on 21q22.3.

K. Yamakawa, R. Hubert, X. Chen, 1995, Human molecular genetics.

BAC and PAC contigs covering 3.5 Mb of the Down syndrome congenital heart disease region between D21S55 and MX1 on chromosome 21.

P. D. de Jong, M. Simon, R. Hubert, 1997, Genomics.

Null mutations in Drosophila Optomotor-blind affect T-domain residues conserved in all Tbx proteins

G. Pflugfelder, Christian Dorner, Yasmin Abassi, 2010, Molecular Genetics and Genomics.