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	1.	Haplotype sharing analysis in affected individuals from nuclear families with at least one affected offspring. [electronic resource] by Van der Meulen, M A te Meerman, G J Producer: 19980219 In: Genetic epidemiology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genomic sharing surrounding alleles identical by descent: effects of genetic drift and population growth. [electronic resource] by te Meerman, G J Van der Meulen, M A Producer: 19980219 In: Genetic epidemiology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Painful decisions: How classifying sensations can change the experience of pain. [electronic resource] by van der Meulen, M A Anton, F Petersen, S Producer: 20180423 In: European journal of pain (London, England) vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Perspectives of identity by descent (IBD) mapping in founder populations. [electronic resource] by Te Meerman, G J Van der Meulen, M A Sandkuijl, L A Producer: 19960327 In: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology vol. 25 Suppl 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Recurrence risk for germinal mosaics revisited. [electronic resource] by van der Meulen, M A van der Meulen, M J te Meerman, G J Producer: 19950628 In: Journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Linkage analysis by two-dimensional DNA typing. [electronic resource] by te Meerman, G J Mullaart, E van der Meulen, M A den Daas, J H Morolli, B Uitterlinden, A G Vijg, J Producer: 19931230 In: American journal of human genetics vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	7.	Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populations. [electronic resource] by de Vries, H G van der Meulen, M A Rozen, R Halley, D J Scheffer, H ten Kate, L P Buys, C H te Meerman, G J Producer: 19960912 In: Human genetics vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type I. [electronic resource] by Verschuuren-Bemelmans, C C Brunt, E R Burton, M Mensink, R G van der Meulen, M A Smit, N H Stolte-Dijkstra, I Buys, C H Scheffer, H Producer: 19960122 In: Human genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testing. [electronic resource] by Dørum, A Møller, P Kamsteeg, E J Scheffer, H Burton, M Heimdal, K R Maehle, L O Hovig, E Tropé, C G van der Hout, A H van der Meulen, M A Buys, C H te Meerman, G J Producer: 19980616 In: European journal of cancer (Oxford, England : 1990) vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)