Amyoplasia congenita-like condition and maternal malathion exposureLINDHOUT, D; HAGEMAN, G.Teratology (Philadelphia, PA). 1987, Vol 36, Num 1, pp 7-9, issn 0040-3709Article

Frontonasal dysplasia, coronal craniosynostosis, pre- and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and variable expression?KWEE, M. L; LINDHOUT, D.Clinical genetics. 1983, Vol 24, Num 3, pp 200-205, issn 0009-9163Article

Premature centromere division (PCD) a dominantly inherited cytogenetic anomalyMADAN, K; LINDHOUT, D; PALAN, A et al.Human genetics. 1987, Vol 77, Num 2, pp 193-196, issn 0340-6717Article

Adult patients with spina bifida cystica : genetic counselling, pregnancy and deliveryRIETBERG, C. C. T; LINDHOUT, D.European journal of obstetrics, gynecology, and reproductive biology. 1993, Vol 52, Num 1, pp 63-70, issn 0301-2115Article

Pregnancy and the risk of teratogenicityLINDHOUT, D; OMTZIGT, J. G. C.Epilepsia (Copenhagen). 1992, Vol 33, pp S41-S48, issn 0013-9580, SUP4Article

H-REFLEX STUDIES IN A FAMILY WITH POSSIBLY X-LINKED NEURONAL CHARCOT-MARIE-TOOTH DISEASEHEIMANS JJ; LINDHOUT D; HUISMAN UW et al.1982; CLINICAL NEUROLOGY AND NEUROSURGERY; ISSN 0303-8467; NLD; DA. 1982; VOL. 84; NO 3; PP. 147-158; BIBL. 25 REF.Article

Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysisDE KOVEL, C. G. F; PINTO, D; BERKOVIC, S. F et al.Epilepsy research. 2010, Vol 89, Num 2-3, pp 286-294, issn 0920-1211, 9 p.Article

Silver-Russell phenotype in a patient with pure trisomy 1 q32.1-q42.1: further delineation of the pure 1 q trisomy syndromeVAN HAELST, M. M; EUSSEN, H. J. F. M. M; VISSCHER, F et al.Journal of medical genetics. 2002, Vol 39, Num 8, pp 582-585, issn 0022-2593Article

No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizuresWINDEMUTH, C; SCHULZ, H; NABBOUT-TARANTINO, R et al.Epilepsy research. 2002, Vol 51, Num 1-2, pp 23-29, issn 0920-1211Article

Management of prenatally detected trisomy 8 mosaicismVAN HAELST, M. M; VAN OPSTAL, D; LINDHOUT, D et al.Prenatal diagnosis. 2001, Vol 21, Num 12, pp 1075-1078, issn 0197-3851Article

Ring chromosome 20 epilepsy syndrome in children: Electroclinical featuresAUGUSTIJN, P. B; PARRA, J; WOUTERS, C. H et al.Neurology. 2001, Vol 57, Num 6, pp 1108-1111, issn 0028-3878Article

Antiepileptic drug regimens and major congenital abnormalities in the offspringSAMREN, E. B; VAN DUIJN, C. M; CHRISTIAENS, G. C. M. L et al.Annals of neurology. 1999, Vol 46, Num 5, pp 739-746, issn 0364-5134Article

The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndromeBOSMA, P. J; JAYANTA ROY CHOWDHURY; NAMITA ROY CHOWDHURY et al.The New England journal of medicine. 1995, Vol 333, Num 18, pp 1171-1175, issn 0028-4793Article

Phenotypic analysis of triphalangeal thumb and associated hand malformationZGURICAS, J; SNIJDERS, P. J. L. M; HOVIUS, S. E. R et al.Journal of medical genetics. 1994, Vol 31, Num 6, pp 462-467, issn 0022-2593Article

Teratogenic effects of antiepileptic drugs : implications for the management of epilepsy in women of childbearing ageLINDHOUT, D; OMTZIGT, J. G. C.Epilepsia (Copenhagen). 1994, Vol 35, pp S19-S28, issn 0013-9580, SUP4Conference Paper

Spectrum of neural-tube defects in 34 infants prenatally exposed to antiepileptic drugsLINDHOUT, D; OMTZIGT, J. G. C; CORNEL, M. C et al.Neurology. 1992, Vol 42, Num 4, pp 111-118, issn 0028-3878, SUP5Article

Individuals with only one allele for a functional insulin receptor have a tendency to hyperinsulinaemia but not to hyperglycaemiaLEKANNE DEPREZ, R. H; POTTER VAN LOON, B. J; VAN DER ZON, G. C. M et al.Diabetologia (Berlin). 1989, Vol 32, Num 10, pp 740-744, issn 0012-186X, 5 p.Article

Fibroblasts from a leprechaum patient have defects in insulin binding and insulin receptor autophosphorylationMAASSEN, J. A; KLINKHAMER, M. P; VAN DER ZON, G. C. M et al.Diabetologia (Berlin). 1988, Vol 31, Num 8, pp 612-617, issn 0012-186XArticle

Concordant cerebral oligodendroglioma in identical twinsROELVINK, N. C. A; KAMPHORST, W; LINDHOUT, D et al.Journal of neurology, neurosurgery and psychiatry. 1986, Vol 49, Num 6, pp 706-708, issn 0022-3050Article

A CASE OF ALS-FTD IN A LARGE FALS PEDIGREE WITH A K171 ANG MUTATIONVAN ES, M. A; DIEKSTRA, F. P; VAN DEN BERG, L. H et al.Neurology. 2009, Vol 72, Num 3, pp 287-288, issn 0028-3878, 2 p.Article

Radiological features of bilateral hereditary micro-epiphyseal dysplasia: a distinct entity in the skeletal dysplasiasMOSTERT, A. K; DIJKSTRA, P. F; VAN HORN, J. R et al.Rofo. Fortschritte auf dem Gebiet der Rontgenstrahlen und der bildgebenden Verfahren. 2002, Vol 174, Num 7, pp 887-892, issn 1438-9029, 6 p.Article

Familial cylindromatosis mimicking tuberous sclerosis complex and confirmation of the cylindromatosis locus, CYLD1, in a large familyVERHOEF, S; SCHRANDER-STUMPEL, C. T. R. M; VUZEVSKI, V. D et al.Journal of medical genetics. 1998, Vol 35, Num 10, pp 841-845, issn 0022-2593Article

Metacarpophalangeal pattern (MCPP) profile analysis in a family with triphalangeal thumbZGURICAS, J; DIJKSTRA, P. F; GELSEMA, E. S et al.Journal of medical genetics. 1997, Vol 34, Num 1, pp 55-62, issn 0022-2593Article

The Dutch uniform multicenter registration system for genetic disorders and malformation syndromesZWAMBORN-HANSSEN, A. M. N; BIJLSMA, J. B; VAN GENNIP, A. H et al.American journal of medical genetics. 1997, Vol 70, Num 4, pp 444-447, issn 0148-7299Article

Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complexVRTEL, R; VERHOEF, S; HOFF, M et al.Journal of medical genetics. 1996, Vol 33, Num 1, pp 47-51, issn 0022-2593Article