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D Lindhout

Showing results (61-70 of 123) with videos related to

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Handchirurgie, Mikrochirurgie, Plastische Chirurgie : Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Handchirurgie : Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Mikrochirurgie Der Peripheren Nerven Und Gefasse : Organ Der V|July 1, 1996
Genetic aspects of polydactylyJ Zguricas, P Heutink, L Heredero, et al.
Nucleic Acids Research|February 25, 1992
Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegiaJ M van den Ouweland, G J Bruining, D Lindhout, et al.
American Journal of Medical Genetics|June 5, 1995
Application of chromosome 16 markers in the differential diagnosis of neuronal ceroid-lipofuscinosisP E Taschner, N de Vos, C E Catsman-Berrevoets, et al.
Lancet (London, England)|January 21, 1995
Somatic mosaicism and clinical variation in tuberous sclerosis complexS Verhoef, R Vrtel, T van Essen, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 29, 1991
[Molecular heterogeneity of congenital forms of insulin resistance]E R van der Vorm, D Lindhout, J M Wit, et al.
The Journal of Biological Chemistry|January 5, 1992
An Arg for Gly substitution at position 31 in the insulin receptor, linked to insulin resistance, inhibits receptor processing and transportE R van der Vorm, G C van der Zon, W Möller, et al.
European Journal of Neurology|June 24, 2016
Epidemiology, pathophysiology and putative genetic basis of carbamazepine- and oxcarbazepine-induced hyponatremiaB Berghuis, G-J de Haan, M P H van den Broek, et al.
American Journal of Medical Genetics|July 1, 1989
Prenatal diagnosis of cystic kidney disease with ventriculomegaly: a report of six cases in two related sibshipsA Reuss, J C den Hollander, M F Niermeijer, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
Familial multiple epiphyseal dysplasia due to a matrilin-3 mutation: further delineation of the phenotype including 40 years follow-upA K Mostert, P F Dijkstra, B R H Jansen, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
A Rett syndrome patient with a ring X chromosome: further evidence for skewing of X inactivation and heterogeneity in the aetiology of the diseaseC Rosenberg, C H Wouters, K Szuhai, et al.
Pageof 13

Showing results (61-70 of 123) with videos related to

Sort By:
Pageof 13
Handchirurgie, Mikrochirurgie, Plastische Chirurgie : Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Handchirurgie : Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Mikrochirurgie Der Peripheren Nerven Und Gefasse : Organ Der V|July 1, 1996
Genetic aspects of polydactylyJ Zguricas, P Heutink, L Heredero, et al.
Nucleic Acids Research|February 25, 1992
Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegiaJ M van den Ouweland, G J Bruining, D Lindhout, et al.
American Journal of Medical Genetics|June 5, 1995
Application of chromosome 16 markers in the differential diagnosis of neuronal ceroid-lipofuscinosisP E Taschner, N de Vos, C E Catsman-Berrevoets, et al.
Lancet (London, England)|January 21, 1995
Somatic mosaicism and clinical variation in tuberous sclerosis complexS Verhoef, R Vrtel, T van Essen, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 29, 1991
[Molecular heterogeneity of congenital forms of insulin resistance]E R van der Vorm, D Lindhout, J M Wit, et al.
The Journal of Biological Chemistry|January 5, 1992
An Arg for Gly substitution at position 31 in the insulin receptor, linked to insulin resistance, inhibits receptor processing and transportE R van der Vorm, G C van der Zon, W Möller, et al.
European Journal of Neurology|June 24, 2016
Epidemiology, pathophysiology and putative genetic basis of carbamazepine- and oxcarbazepine-induced hyponatremiaB Berghuis, G-J de Haan, M P H van den Broek, et al.
American Journal of Medical Genetics|July 1, 1989
Prenatal diagnosis of cystic kidney disease with ventriculomegaly: a report of six cases in two related sibshipsA Reuss, J C den Hollander, M F Niermeijer, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
Familial multiple epiphyseal dysplasia due to a matrilin-3 mutation: further delineation of the phenotype including 40 years follow-upA K Mostert, P F Dijkstra, B R H Jansen, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
A Rett syndrome patient with a ring X chromosome: further evidence for skewing of X inactivation and heterogeneity in the aetiology of the diseaseC Rosenberg, C H Wouters, K Szuhai, et al.
Pageof 13