TY  - JOUR
A1  - Vortkamp, Andrea
A1  - Gessler, Manfred
A1  - Grzeschik, Karl-Heinz
T1  - GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families
N2  - No abstract available
Y1  - 1991
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30100
ER  - 
TY  - JOUR
A1  - Vortkamp, Andrea
A1  - Franz, Thomas
A1  - Gessler, Manfred
A1  - Grzeschik, Karl-Heinz
T1  - Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt)
N2  - No abstract available
Y1  - 1992
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30166
ER  - 
TY  - JOUR
A1  - Vortkamp, Andrea
A1  - Gessler, Manfred
A1  - Paslier, D. Le
A1  - Elaswarapu, R.
A1  - Smith, S.
A1  - Grzeschik, Karl-Heinz
T1  - Isolation of a yeast artificial chromosome contig spanning the Greig cephalopolysyndactyly syndrome (GCPS) gene region
N2  - Disruption of the zinc finger gene GLI3 has been shown to be the cause of Greig cephalopolysyndactyly syndrome (GCPS), at least in some GCPS translocation patients. To characterize this genomic region on human chromosome 7p13, we have isolated a VAC contig of more than 1000 kb including the GLI3 gene. In this contig the gene itself spans at least 200-250 kb. A CpG island is located in the vicinity of the 5' region of the known GLI3 cDNA, implying a potential promoter region.
Y1  - 1994
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30182
ER  -