Body wall defects in two sibsHELDERMAN-VAN DEN ENDEN, A. T. J. M; BARTELINGS, M. M; VAN KAMP, I. L et al.American journal of medical genetics. 1997, Vol 73, Num 1, pp 15-18, issn 0148-7299Article

Monozygotic twin brothers with the fragile X syndrome : different CGG repeats and different mental capacitiesHELDERMAN-VAN DEN ENDEN, A. T. J. M; MAASWINKEL-MOOIJ, P. D; HOOGENDOORN, E et al.Journal of medical genetics. 1999, Vol 36, Num 3, pp 253-257, issn 0022-2593Article

Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies : a genotype -phenotype correlation studyDIERICK, Ines; BAETS, Jonathan; FISCHER, Dirk et al.Brain. 2008, Vol 131, pp 1217-1227, issn 0006-8950, 11 p., 5Article

A near false-negative finding of mosaic trisomy 21 : A cautionary taleBEVERSTOCK, G. C; HANSSON, K; HELDERMAN-VAN DEN ENDEN, A. T. J. M et al.Prenatal diagnosis. 1998, Vol 18, Num 7, pp 742-746, issn 0197-3851Article