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dai: 074039210
scopus: 35388704200

Lindhout, D.

(Dick Lindhout)

Supervisor (promotor) of 7 dissertations


mutation patient family analysis genet study antiepileptic drugs mother syndrome parent tsc 1 gene ahi 1 mutations antiepileptic abnormality disease cancer joubert syndrome tsc 2 gene joubert table allele control children tuberous sclerosis carrier netherland mosaicism msx 1 cleft tuberou epilepsy sclerosis child hearing deletion valproate folic smoking hnpcc msh 6 mutation genetic 4/4 genotype father chromosome university colorectal pregnancy defect dutch caffeine combination antiepileptic drug regimens folate pedigree department phenobarbital expression article phenotype endometrial hearing loss tsc 1 x /xa tsc patients / european journal result center ofc risk carbamazepine dystrophy number sequence nphp 1 deletions reference endometrial cancer association carcinoma offspring periconceptional period




10 Most Recent Publications

Incomplete segregation of MYH11 variants with thoracic aortic aneurysms and dissections and patent ductus arteriosus (Article)
Harakalova, M. Smagt, J.J. van der Wessels, M.W. Baars, H.F. Weiss, M.M. Pals, G. Golmard, L. Jeunemaitre, X. Lindhout, D. Cuppen, E. Baas, A.F. Kovel, C.G.F. de Slot, R.V. Poot, M. Nijman, I.J. Medic, J. Joziasse, I.C. Deckers, J.W. Roos-Hesselink, J.W.
2013-05-01
Is hearing loss a feature of Joubert syndrome, a ciliopathy? (Article)
Kroes, H.Y. Zanten, B.G.A. Ru, S.A. de Boon, M. Mancini, G.M.S. Knaap, M.S. van der Poll-The, B.T. Lindhout, D.
2010-09-01
The MSX1 allele 4 homozygous child exposed to smoking at periconception is most sensitive in developing nonsyndromic orofacial clefts (Article)
Boogaard, M.J.H. Costa, D. Krapels, I.P.C. Liu, F. Duijn, C.M. van Sinke, R.J. Lindhout, D. Streegers-Theunissen, R.P.M.
2008-10-20
DNA analysis of AHI1, NPHP1 and CYCLIN D1 in Joubert syndrome patients from the Netherlands (Article)
Kroes, H.Y. Zon, P.H.A. van Maas, S.M. Cobben, J.M. Nef, J.E.E. de Lindhout, D. Sinke, R.J. Putte, D.F. van de Nelen, M.R. Nievelstein, R.J. Wittebol-Post, D. Nieuwenhuizen, O. van Mancini, G.M.S. Knaap, M.S. van der Kwee, M.L.
2008-01-01
Genetic risk estimation by healthcare professionals (Article)
Bonke, B. Tibben, A. Lindhout, D. Clarke, A.J. Stijnen, Th.
2005-01-01
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree (Article)
Wagner, A. Krimpen, C. van Breuning, M.H. Meer, C. van der Vasen, H.F. Niermeijer, M.F. Lindhout, D. Hendriks, Y. Meijers-Heijboer, E.J. Wijnen, J. Leeuw, W.J. de Morreau, H. Hofstra, R. Tops, C. Cornelisse, C.J. Zwinderman, A.H. Bik, E. Brocker-Vriends, A.H. Fodde, R.
2001-01-01
Anti-epileptic drug regimens and major congenital abnormalities in the offspring (Article)
Samren, E.B. Duijn, C.M. van Christiaens, C.G.M.L. Hofman, A. Lindhout, D.
1999-01-01
Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation (Article)
Verhoef, S. Tempelaars, A. Slegtenhorst, M.A. van Bakker, L. Wang, Q. Wessels, M.W. Nellist, M.D. Bakker, R. Lindhout, D. Halley, D.J.J. Ouweland, A.M.W. van den
1999-01-01
High rate of mosaicism in tuberous sclerosis complex (Article)
Verhoef, S. Ouweland, A.M.W. van den Halley, D.J.J. Bakker, L. Tempelaars, A.M. Hesseling-Janssen, A.L. Mazurczak, T. Jozwiak, S. Zonnenberg, B.A. Essen, A.J. van Lindhout, D.
1999-01-01
Maternal use of antiepileptic drugs and the risk of major congenital malformations: a joint European prospective study of human teratogenesis associated with maternal epilepsy. (Article)
Samren, E.B. Duijn, C.M. van Meinardi, H. Grobbee, D.E. Lindhout, D. Hofman, A. Koch, S. Hiilesma, V.K. Klepel, H. Bardy, A.H. Mannegetta, B. Deichl, A.W. Gaily, E. Granstrom, M.L.
1997-01-01