Prehistoric and Roman gullying in the european loess belt : a case study from central Belgium
VANWALLEGHEM, T, BORK, H. R, POESEN, J, DOTTERWEICH, M, SCHMIDTCHEN, G, DECKERS, J, SCHEERS, S, MARTENS, M
Published in Holocene (Sevenoaks) (01.04.2006)
Published in Holocene (Sevenoaks) (01.04.2006)
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Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics
Rooms, L, Reyniers, E, Wuyts, W, Storm, K, Van Luijk, R, Scheers, S, Wauters, J, Van Den Ende, J, Biervliet, M, Eyskens, F, Van Goethem, G, Laridon, A, Ceulemans, B, Courtens, W, Kooy, RF
Published in Clinical genetics (01.01.2006)
Published in Clinical genetics (01.01.2006)
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The molecular basis of the folate-sensitive fragile site FRA11A at 11q13
Debacker, K., Winnepenninckx, B., Longman, C., Colgan, J., Tolmie, J., Murray, R., van Luijk, R., Scheers, S., FitzPatrick, D., Kooy, F.
Published in Cytogenetic and genome research (01.01.2007)
Published in Cytogenetic and genome research (01.01.2007)
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Prehistoric and Roman gullying in the European oess belt: a case study from central Belgium
Vanwalleghem, T., Bork, H. R., Poesen, J., Dotterweich, M., Schmidtchen, G., Deckers, J., Scheers, S., Martens, M.
Published in Holocene (Sevenoaks) (01.04.2006)
Published in Holocene (Sevenoaks) (01.04.2006)
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Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation-dependent probe amplification (MLPA)
Rooms, Liesbeth, Reyniers, Edwin, Luijk, Rob van, Scheers, Stefaan, Wauters, Jan, Ceulemans, Berten, Van Den Ende, Jenneke, Van Bever, Yolande, Kooy, R. Frank
Published in Human mutation (01.01.2004)
Published in Human mutation (01.01.2004)
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Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype
van Bever, Yolande, Rooms, Liesbeth, Laridon, Annick, Reyniers, Edwin, van Luijk, Rob, Scheers, Stefaan, Wauters, Jan, Kooy, R. Frank
Published in American journal of medical genetics. Part A (15.05.2005)
Published in American journal of medical genetics. Part A (15.05.2005)
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FRA18C: a new aphidicolin-inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakage
Debacker, Kim, Winnepenninckx, Birgitta, Ben-Porat, Neta, FitzPatrick, David, Van Luijk, Rob, Scheers, Stefaan, Kerem, Batsheva, Frank Kooy, R
Published in Journal of medical genetics (01.05.2007)
Published in Journal of medical genetics (01.05.2007)
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Short Report: Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics
Rooms, L, Reyniers, E, Wuyts, W, Storm, K, R van Luijk, Scheers, S, Wauters, J, van den Ende, J, Biervliet, M, Eyskens, F, G van Goethem, Laridon, A, Ceulemans, B, Courtens, W, Kooy, R F
Published in Clinical genetics (01.01.2006)
Published in Clinical genetics (01.01.2006)
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Control device, flow-through heater, and method for controlling a flow-through heater
BERGE VAN DEN ROB, VERDAASDONK BART, WIERENGA HENDRIK JACOB LAMMERT, SCHEERS ARJAN, RUTTEN TIM
Year of Publication 28.11.2017
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Year of Publication 28.11.2017
Patent
Properties of N-butyl-N-methyl-pyrrolidinium Bis(trifluoromethanesulfonyl) Imide Based Electrolytes as a Function of Lithium Bis(trifluoromethanesulfonyl) Imide Doping
Kim, Jae-Kwang, Lim, Du-Hyun, Scheers, Johan, Pitawala, Jagath, Wilken, Susanne, Johansson, Patrik, Ahn, Jou-Hyeon, Matic, Aleksandar, Jacobsson, Per
Published in 전기화학회지 (2011)
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Published in 전기화학회지 (2011)
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