Pharmacogenetics and drug interactions : role in antiepileptic-drug-induced teratogenesisLINDHOUT, D.Neurology. 1992, Vol 42, Num 4, pp 43-47, issn 0028-3878, SUP5Article

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

THE JOUBERT SYNDROME ASSOCIATED WITH BILATERAL CHORIORETINAL COLOBOMALINDHOUT D; BARTH PG; VALK J et al.1980; EUROP. J. PEDIATR.; DEU; DA. 1980; VOL. 134; NO 2; PP. 173-176; BIBL. 15 REF.Article

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

Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patientsLETTEBOER, T. G. W; ZEWALD, R. A; KAMPING, E. J et al.Human genetics. 2005, Vol 116, Num 1-2, pp 8-16, issn 0340-6717, 9 p.Article

Gestation-induced changes in lamotrigine pharmacokinetics: A monotherapy studyDE HAAN, G-J; EDELBROEK, P; SEGERS, J et al.Neurology. 2004, Vol 63, Num 3, pp 571-573, issn 0028-3878, 3 p.Article

Different phenotypic expression in relatives with Fabry disease caused by a W226X mutationKNOL, I. E; AUSEMS, M. G. E. M; LINDHOUT, D et al.American journal of medical genetics. 1999, Vol 82, Num 5, pp 436-439, issn 0148-7299Article

Linkage to markers for the chromosome region 17q12.q21 in 13 dutch breast cancer kindredsDEVILEE, P; CORNELIS, R. S; CORNELISSE, C. J et al.American journal of human genetics. 1993, Vol 52, Num 4, pp 730-735, issn 0002-9297Article

Prenatal ultrasonographic diagnosis of radial-ray reduction malformationsBRONS, J. T. Z; VAN DER HARTEN, H. J; VAN DEIJN, H. P et al.Prenatal diagnosis. 1990, Vol 10, Num 5, pp 279-288, issn 0197-3851, 10 p.Article

The diagnostic management of newborns with congenital contractures: a nosologic study of 75 casesHAGEMAN, G; IPPEL, E. P. F; BEEMER, F. A et al.American journal of medical genetics. 1988, Vol 30, Num 4, pp 883-904, issn 0148-7299Article

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

Complex cardiac defect with hypoplastic right ventricle in a fetus with valproate exposureTEN BERG, K; VAN OPPEN, A. C. C; NIKKELS, P. G. J et al.Prenatal diagnosis. 2005, Vol 25, Num 2, pp 156-158, issn 0197-3851, 3 p.Article

Atypical HNPCC owing to MSH6 germline mutations : analysis of a large Dutch pedigreeWAGNER, A; HENDRIKS, Y; LINDHOUT, D et al.Journal of medical genetics. 2001, Vol 38, Num 5, pp 318-322, issn 0022-2593Article

Genome search for susceptibility loci of common idiopathic generalised epilepsiesSANDER, T; SCHULZ, H; VILLE, D et al.Human molecular genetics (Print). 2000, Vol 9, Num 10, pp 1465-1472, issn 0964-6906Article

A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (epm2)SERRATOSA, J. M; GOMEZ-GARREL, P; TOPCU, M et al.Human molecular genetics (Print). 1999, Vol 8, Num 2, pp 345-352, issn 0964-6906Article

Malignant pancreatic tumour within the spectrum of tuberous sclerosis complex in childhoodVERHOEF, S; VAN DIEMEN-STEENVOORDE, R; LIPS, K et al.European journal of pediatrics. 1999, Vol 158, Num 4, pp 284-287, issn 0340-6199Article

Mutational spectrum of the TSC 1 gene in a cohort of 225 tuberous sclerosis complex patients : no evidence for genotype-phenotype correlationVAN SLEGTENHORST, M; VERHOEF, S; VAN DEN OUWELAND, A et al.Journal of medical genetics. 1999, Vol 36, Num 4, pp 285-289, issn 0022-2593Article

Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34VAN SLEGTENHORST, M; DE HOOGT, R; BURLEY, M et al.Science (Washington, D.C.). 1997, Vol 277, Num 5327, pp 805-808, issn 0036-8075Article

Severe limb abnormalities : analysis of a cluster of five cases born during a period of 45 daysVAN DEN ANKER, J. N; VAN VUGHT, E. E; ZANDWIJKEN, G. R. J et al.American journal of medical genetics. 1993, Vol 45, Num 5, pp 659-667, issn 0148-7299Article

An Arg for Gly substitution at position 31 in the insulin receptor, linked to insulin resistance, inhibits receptor processing and transportVAN DER VORM, E. R; VAN DER ZON, G. C. M; MÖLLER, W et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 1, pp 66-71, issn 0021-9258Article

Prenatal analysis of insulin receptor autophosphorylation in a family with leprechaunismMAASSEN, J. A; LINDHOUT, D; REUSS, A et al.Prenatal diagnosis. 1990, Vol 10, Num 1, pp 13-16, issn 0197-3851, 4 p.Article

Fibrodysplasia ossificans progressiva: current concepts and the role of CT in acute changesLINDHOUT, D; GOLDING, R. P; VAN AMERONGEN, A. H. M. T et al.Pediatric radiology. 1985, Vol 15, Num 3, pp 211-213, issn 0301-0449Article