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Entries: 1-4  
Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia
Authors: Ott, C. E.; Leschik, G.; Trotier, F.; Brueton, L.; Brunner, H. G.; Brussel, W.; Guillen-Navarro, E.; Haase, C.; Kohlhase, J.; Kotzot, D.; Lane, A.; Lee-Kirsch, M. A.; Morlot, S.; Simon, M. E.; Steichen-Gersdorf, E.; Tegay, D. H.; Peters, H.; Mundlos, S.; Klopocki, E.
Date of Publication (YYYY-MM-DD): 2010-06-03
Title of Journal: Human Mutation
Volume: 31
Issue / Number: 8
Start Page: E1587
End Page: 93
Document Type: Article
ID: 539733.0
Full text / Content available
C-terminally truncated kindlin-1 leads to abnormal adhesion and migration of keratinocytes
Authors: Has, C.; Ludwig, R. J.; Herz, C.; Kern, J. S.; Ussar, S.; Ochsendorf, F. R.; Kaufmann, R.; Schumann, H.; Kohlhase, J.; Bruckner-Tuderman, L.
Date of Publication (YYYY-MM-DD): 2008-11
Title of Journal: British Journal of Dermatology
Volume: 159
Issue / Number: 5
Start Page: 1192
End Page: 1196
Document Type: Article
ID: 394940.0
Interaction of the developmental regulator SALL1 with UBE2I and SUMO-1
Authors: Netzer, C.; Bohlander, S. K.; Rieger, L.; Muller, S.; Kohlhase, J.
Date of Publication (YYYY-MM-DD): 2002-08-30
Title of Journal: Biochemical and Biophysical Research Communications
Volume: 296
Issue / Number: 4
Start Page: 870
End Page: 876
Document Type: Article
ID: 41777.0
Molecular cloning of a SALL1-related pseudogene and mapping to chromosome Xp11.2.
Authors: Kohlhase, J.; Koehler, A.; Jaeckle, H.; Engel, W.; Stick, R.
Date of Publication (YYYY-MM-DD): 1999
Title of Journal: Cytogenetics and Cell Genetics
Volume: 84
Start Page: 31
End Page: 34
Document Type: Article
ID: 227081.0
Entries: 1-4  
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