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Publications by Wilcken, B.

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Journal article

Kamp, J. M. van de; Betsalel, O. T.; Mercimek-Mahmutoglu, S.; Abulhoul, L.; Grünewald, S.; Anselm, I.; Azzouz, H.; Bratkovic, D.; Brouwer, A. de; Hamel, B.; Kleefstra, T.; Yntema, H.; Campistol, J.; Vilaseca, M. A.; Cheillan, D.; Hooghe, M. D'; Diogo, L.; Garcia, P.; Valongo, C.; Fonseca, M.; Frints, S.; Wilcken, B.; Haar, S.; Meijers-Heijboer, H. E. von der; Hofstede, F.; Johnson, D.; Kant, S. G.; Lion-Francois, L.; Pitelet, G.; Longo, N.; Maat-Kievit, J. A.; Monteiro, J. P.; Munnich, A.; Muntau, Ania Carolina; Nassogne, M. C.; Osaka, H.; Ounap, K.; Pinard, J. M.; Quijano-Roy, S.; Poggenburg, I.; Poplawski, N.; Abdul-Rahman, O.; Ribes, A.; Arias, A.; Yaplito-Lee, J.; Schulze, A.; Schwartz, C. E.; Schwenger, S.; Soares, G.; Sznajer, Y.; Valayannopoulos, V.; Esch, H. Van; Waltz, S.; Wamelink, M. M. C.; Pouwels, P. J. W.; Errami, A.; Knaap, M. S. van der; Jakobs, C.; Mancini, G. M.; Salomons, G. S. (July 2013): Phenotype and genotype in 101 males with X-linked creatine transporter deficiency. In: Journal of Medical Genetics, Vol. 50, No. 7: pp. 463-472 [PDF, 968kB]

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