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Programme
“Connective Tissue Genetics” |
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08.45
|
Registration | |
|
09.15
|
Welcome | |
| CHAIR: A. DE PAEPE (UG), M. PARMENTIER (ULB) | ||
| 09.30-10.00 | Bone in balance and imbalance |
W. Van Hul
(Antwerpen)
|
| 10.00-10.30 | Multiple roles of the elastic matrix in morphogenesis and homeostasis |
F. Ramirez (New
York)
|
| 10.30-11.15 | Coffee break and poster session |
|
| CHAIR: G. VAN CAMP (UA), M. VIKKULA (UCL) | ||
| 11.15-11.45 | Epidermolysis bullosa : from genes to symptoms and therapy |
L.
Bruckner-Tuderman(Freiburg)
|
| 11.45-12.15 | The callipyge phenotype : paradigm of non-Mendelian inheritance |
M. Georges
(Liège)
|
| 12.15-12.45 | Mutation detection and identification using Applied Biosystems |
M. Wijker (ABI)
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| 12.45-13.15 | Lunch and poster session |
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| 13.15-14.15 | General Assembly |
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| CHAIR: M. ABRAMOWICZ (ULB), K. KEYMOLEN (VUB) | ||
| 14.15-15.30 | Selected oral communications |
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|
14.15
|
N. De Temmerman : Disease-causing CTG triplet repeat instability in human gametes and preimplantation embryos |
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|
14.30
|
N. Maas : The analysis of 4p chromosomal abnormalities using micro-array CGH | |
|
14.45
|
L. Meeus : Characterization of a novel loss-of-function mutation of PAX8 in a familial case of congenital hypothyroidism by dysgenesis | |
|
15.00
|
H. Peeters : PA26 is a cause of human heterotaxia |
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|
15.15
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C. Spits : Multiplex-PCR for polymorphic markers linked to FBN1-gene : application in PGD for Marfan syndrome | |
| 15.30-16.00 | Coffee break and poster session | |
| CHAIR: V. BOURS (ULG), K. DEVRIENDT (KUL) | ||
| 16.00-16.30 | Scar-free wound healing | M. Ferguson (Manchester) |
| 16.30-17.00 | Novel proteome strategies : their potential impact on biomedical research and medicine | J. Vandekerckhove (Gent) |
|
17.15
|
End of the meeting | |