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D Lindhout

Showing results (31-40 of 123) with videos related to

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European Journal of Pediatrics|August 1, 1980
The Joubert syndrome associated with bilateral chorioretinal colobomaD Lindhout, P G Barth, J Valk, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 26, 2001
[From gene to disease; TSC1 and TSC2 genes and tuberous sclerosis complex]S Verhoef, D Lindhout, D J Halley, et al.
FEBS Letters|July 29, 1996
A mutation which disrupts the hydrophobic core of the signal peptide of bilirubin UDP-glucuronosyltransferase, an endoplasmic reticulum membrane protein, causes Crigler-Najjar type IIJ Seppen, E Steenken, D Lindhout, et al.
European Journal of Clinical Pharmacology|January 1, 1992
The disposition of valproate and its metabolites in the late first trimester and early second trimester of pregnancy in maternal serum, urine, and amniotic fluid: effect of dose, co-medication, and the presence of spina bifidaJ G Omtzigt, H Nau, F J Los, et al.
Acta Neurologica Scandinavica. Supplementum|January 1, 1992
In search for genes predisposing to epilepsy: motives and methodsD Lindhout, T Sander, D J Halley, et al.
Prenatal Diagnosis|December 18, 2001
Management of prenatally detected trisomy 8 mosaicismM M van Haelst, D Van Opstal, D Lindhout, et al.
Lancet (London, England)|November 3, 1990
Convulsions in epileptic women after administration of prostaglandin E2 derivativeH Brandenburg, M G Jahoda, J W Wladimiroff, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 1, 2002
[From gene to disease; progressive myoclonus epilepsy of Unverricht-Lundborg and mutations in the cystatin B gene]G J de Haan, D J J Halley, W H Deelen, et al.
Neuropediatrics|February 1, 1987
The heterogeneity of the Pena-Shokeir syndromeG Hageman, J Willemse, B A van Ketel, et al.
Plastic and Reconstructive Surgery|March 26, 1998
Genetics of limb development and congenital hand malformationsJ Zguricas, W F Bakker, H Heus, et al.
Pageof 13

Showing results (31-40 of 123) with videos related to

Sort By:
Pageof 13
European Journal of Pediatrics|August 1, 1980
The Joubert syndrome associated with bilateral chorioretinal colobomaD Lindhout, P G Barth, J Valk, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 26, 2001
[From gene to disease; TSC1 and TSC2 genes and tuberous sclerosis complex]S Verhoef, D Lindhout, D J Halley, et al.
FEBS Letters|July 29, 1996
A mutation which disrupts the hydrophobic core of the signal peptide of bilirubin UDP-glucuronosyltransferase, an endoplasmic reticulum membrane protein, causes Crigler-Najjar type IIJ Seppen, E Steenken, D Lindhout, et al.
European Journal of Clinical Pharmacology|January 1, 1992
The disposition of valproate and its metabolites in the late first trimester and early second trimester of pregnancy in maternal serum, urine, and amniotic fluid: effect of dose, co-medication, and the presence of spina bifidaJ G Omtzigt, H Nau, F J Los, et al.
Acta Neurologica Scandinavica. Supplementum|January 1, 1992
In search for genes predisposing to epilepsy: motives and methodsD Lindhout, T Sander, D J Halley, et al.
Prenatal Diagnosis|December 18, 2001
Management of prenatally detected trisomy 8 mosaicismM M van Haelst, D Van Opstal, D Lindhout, et al.
Lancet (London, England)|November 3, 1990
Convulsions in epileptic women after administration of prostaglandin E2 derivativeH Brandenburg, M G Jahoda, J W Wladimiroff, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 1, 2002
[From gene to disease; progressive myoclonus epilepsy of Unverricht-Lundborg and mutations in the cystatin B gene]G J de Haan, D J J Halley, W H Deelen, et al.
Neuropediatrics|February 1, 1987
The heterogeneity of the Pena-Shokeir syndromeG Hageman, J Willemse, B A van Ketel, et al.
Plastic and Reconstructive Surgery|March 26, 1998
Genetics of limb development and congenital hand malformationsJ Zguricas, W F Bakker, H Heus, et al.
Pageof 13