The mouse Arhgef6gene: cDNA sequence, expression analysis, and chromosome assignmentKUTSCHE, K; GAL, A.Cytogenetics and cell genetics. 2001, Vol 95, Num 3-4, pp 196-201, issn 0301-0171Article

Refining the phenotype of α-1a Tubulin (TUBA1A) mutation in patients with classical lissencephalyMORRIS-ROSENDAHL, D. J; NAJM, J; VASCONCELOS, C et al.Clinical genetics. 2008, Vol 74, Num 5, pp 425-433, issn 0009-9163, 9 p.Article

Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndromeSCHULZ, A. L; ALBRECHT, B; KÖNIG, R et al.Clinical genetics. 2008, Vol 73, Num 1, pp 62-70, issn 0009-9163, 9 p.Article

Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epitheliumKUTSCHE, K; GLAUNER, E; ALTHAUS, C et al.Cytogenetics and cell genetics. 2000, Vol 91, Num 1-4, pp 141-147, issn 0301-0171Article

Microlithographic patterning of polythiophene filmsKUTSCHE, K; TARGOVE, J; HAALAND, P et al.Journal of applied physics. 1993, Vol 73, Num 5, pp 2602-2604, issn 0021-8979Article

Microphthalmia with linear skin defects syndrome (MLS): a male with a mosaic paracentric inversion of XpKUTSCHE, K; WERNER, W; BARTSCH, O et al.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 297-302, issn 1424-8581, 6 p.Article

Predetermined chromosomal deletion encompassing the Nf-1 geneSCHLAKE, T; SCHUPP, I; KUTSCHE, K et al.Oncogene (Basingstoke). 1999, Vol 18, Num 44, pp 6078-6082, issn 0950-9232Article