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American Journal of Medical Genetics|February 7, 1998
Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50)S Claes, A Vogels, M Holvoet, et al.American Journal of Medical Genetics|July 9, 1999
Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1S Claes, P Volcke, K Devriendt, et al.American Journal of Medical Genetics|January 11, 1996
Ichthyosis-characteristic appearance-mental retardation syndrome with distinct histological skin abnormalitiesK Devriendt, J van den Oord, R De Vos, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|March 31, 1994
Intractable asphyxia at birth: analysis of the underlying conditionsH Devlieger, J Jaeken, P Moerman, et al.Annales De Genetique|January 5, 2002
Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosomeI Witters, P Moerman, D Louwagie, et al.European Journal of Clinical Pharmacology|November 12, 2005
O-demethylation of tramadol in the first months of lifeKarel Allegaert, J N Van den Anker, R Verbesselt, et al.Clinical Genetics|November 15, 2002
Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11)P Debeer, R Mols, C Huysmans, et al.Clinical Genetics|May 1, 1996
Cohen syndrome: the clinical symptoms and stigmata at a young ageJ P Fryns, E Legius, K Devriendt, et al.Prenatal Diagnosis|May 10, 2002
Prenatal findings in a monozygotic twin pregnancy with Costello syndromeT Van den Bosch, D Van Schoubroeck, J P Fryns, et al.Genomics|December 1, 1996
Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasiaP M Groenen, E Garcia, P Debeer, et al.Pageof 105