Incorrect specification of marker allele frequencies: effects on linkage analysis.

Por Freimer, N B, Sandkuijl, L A, Blower, S M
Publicado em 1993

Linkage investigation of three putative tuberous sclerosis determining loci on chromosomes 9q, 11q, and 12q. The Tuberous Sclerosis Collaborative Group.

Por Sampson, J R, Janssen, L A, Sandkuijl, L A
Publicado em 1992

Linkage-disequilibrium mapping of disease genes by reconstruction of ancestral haplotypes in founder populations.

Por Service, S K, Lang, D W, Freimer, N B, Sandkuijl, L A
Publicado em 1999

Computer simulation of linkage and heterogeneity in tuberous sclerosis: a critical evaluation of the collaborative family data.

Por Janssen, L A, Sandkuijl, L A, Sampson, J R, Halley, D J
Publicado em 1992

Covariate-dependent age-at-onset distributions for Huntington disease.

Por Krawczak, M, Bockel, B, Sandkuijl, L, Thies, U, Fenton, I, Harper, P S
Publicado em 1991

An apolipoprotein CIII haplotype protective against hypertriglyceridemia is specified by promoter and 3' untranslated region polymorphisms.

Por Dammerman, M, Sandkuijl, L A, Halaas, J L, Chung, W, Breslow, J L
Publicado em 1993

Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family

Por de Kovel, C G F, Hol, F, Heister, J, Willemen, J, Sandkuijl, L, Franke, B, Padberg, G
Publicado em 2004

Dutch patients with glycogen storage disease type II show common ancestry for the 525delT and del exon 18 mutations

Por Ausems, M., ten, B, Sandkuijl, L., Kroos, M., Bardoel, A., Roumelioti, K., Reuser, A., Sinke, R., Wijmenga, C.
Publicado em 2001

Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneity.

Por Heutink, P, Haitjema, T, Breedveld, G J, Janssen, B, Sandkuijl, L A, Bontekoe, C J, Westerman, C J, Oostra, B A
Publicado em 1994

Linkage studies on Gilles de la Tourette syndrome: what is the strategy of choice?

Por Heutink, P, van de Wetering, B J, Pakstis, A J, Kurlan, R, Sandor, P, Oostra, B A, Sandkuijl, L A
Publicado em 1995

A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD)

Por van der Maarel, S. M, Deidda, G., Lemmers, R., Bakker, E., van der Wielen, M. J R, Sandkuijl, L., Hewitt, J., Padberg, G., Frants, R.
Publicado em 1999

MRI screening of kindred at risk of developing paragangliomas: support for genomic imprinting in hereditary glomus tumours.

Por van Gils, A. P., van der Mey, A. G., Hoogma, R. P., Sandkuijl, L. A., Maaswinkel-Mooy, P. D., Falke, T. H., Pauwels, E. K.
Publicado em 1992

The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27.

Por Leegwater, P A, Könst, A A, Kuyt, B, Sandkuijl, L A, Naidu, S, Oudejans, C B, Schutgens, R B, Pronk, J C, van der Knaap, M S
Publicado em 1999

Significant linkage disequilibrium between the Huntington disease gene and the loci D4S10 and D4S95 in the Dutch population.

Por Skraastad, M I, Van de Vosse, E, Belfroid, R, Höld, K, Vegter-van der Vlis, M, Sandkuijl, L A, Bakker, E, van Ommen, G J
Publicado em 1992

Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes.

Por Mitchison, H M, O'Rawe, A M, Taschner, P E, Sandkuijl, L A, Santavuori, P, de Vos, N, Breuning, M H, Mole, S E, Gardiner, R M, Järvelä, I E
Publicado em 1995

Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.

Por Boerman, R H, Ophoff, R A, Links, T P, van Eijk, R, Sandkuijl, L A, Elbaz, A, Vale-Santos, J E, Wintzen, A R, van Deutekom, J C, Isles, D E
Publicado em 1995

Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome.

Por Meijers-Heijboer, E J, Sandkuijl, L A, Brunner, H G, Smeets, H J, Hoogeboom, A J, Deelen, W H, van Hemel, J O, Nelen, M R, Smeets, D F, Niermeijer, M F
Publicado em 1992

Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter

Por Wijmenga, C., Sandkuijl, L. A., Moerer, P., van der Boorn, N., Bodrug, S. E., Ray, P. N., Brouwer, O. F., Murray, J. C., van Ommen, G. J. B., Padberg, G. W., Frants, R. R.
Publicado em 1992

A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q

Por Bakker, S. C., Meulen, E. M. van der, Buitelaar, J. K., Sandkuijl, L. A., Pauls, D. L., Monsuur, A. J., Slot, R. van ‘t, Minderaa, R. B., Gunning, W. B., Pearson, P. L., Sinke, R. J.
Publicado em 2003

Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group.

Por de Vries, B B, van den Ouweland, A M, Mohkamsing, S, Duivenvoorden, H J, Mol, E, Gelsema, K, van Rijn, M, Halley, D J, Sandkuijl, L A, Oostra, B A, Tibben, A, Niermeijer, M F
Publicado em 1997