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Neuromuscular Disorders : NMD|January 1, 1991
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research GroupP Raeymaekers, V Timmerman, E Nelis, et al.Genomics|October 1, 1990
Assignment of X-linked hydrocephalus to Xq28 by linkage analysisP J Willems, I Dijkstra, B J Van der Auwera, et al.Journal of Affective Disorders|May 1, 1997
A chromosome 18 genetic linkage study in three large Belgian pedigrees with bipolar disorderS Claes, P Raeymaekers, M Van den Broeck, et al.Genomics|April 1, 1991
Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22P J Willems, J Hendrickx, B J Van der Auwera, et al.Archives of Neurology|June 1, 1990
Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the same familyP J Willems, L Vits, R J Wanders, et al.American Journal of Medical Genetics|July 14, 2000
A European multicenter association study of HTR2A receptor polymorphism in bipolar affective disorderI Massat, D Souery, O Lipp, et al.Journal of Affective Disorders|April 13, 2000
Linkage of mood disorders with D2, D3 and TH genes: a multicenter studyA Serretti, F Macciardi, C Cusin, et al.Pageof 5