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M A van der Meulen

Showing results (1-10 of 9) with videos related to

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Genetic Epidemiology|January 1, 1997
Genomic sharing surrounding alleles identical by descent: effects of genetic drift and population growthG J te Meerman, M A Van der Meulen
Genetic Epidemiology|January 1, 1997
Haplotype sharing analysis in affected individuals from nuclear families with at least one affected offspringM A Van der Meulen, G J te Meerman
European Journal of Pain (London, England)|June 3, 2017
Painful decisions: How classifying sensations can change the experience of painM A van der Meulen, F Anton, S Petersen
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|November 1, 1995
Perspectives of identity by descent (IBD) mapping in founder populationsG J Te Meerman, M A Van der Meulen, L A Sandkuijl
Journal of Medical Genetics|February 1, 1995
Recurrence risk for germinal mosaics revisitedM A van der Meulen, M J van der Meulen, G J te Meerman
American Journal of Human Genetics|December 1, 1993
Linkage analysis by two-dimensional DNA typingG J te Meerman, E Mullaart, M A van der Meulen, et al.
Human Genetics|September 1, 1996
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 populationsH G de Vries, M A van der Meulen, R Rozen, et al.
Human Genetics|December 1, 1995
Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type IC C Verschuuren-Bemelmans, E R Brunt, M Burton, et al.
European Journal of Cancer (Oxford, England : 1990)|June 9, 1998
A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testingA Dørum, P Møller, E J Kamsteeg, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Genetic Epidemiology|January 1, 1997
Genomic sharing surrounding alleles identical by descent: effects of genetic drift and population growthG J te Meerman, M A Van der Meulen
Genetic Epidemiology|January 1, 1997
Haplotype sharing analysis in affected individuals from nuclear families with at least one affected offspringM A Van der Meulen, G J te Meerman
European Journal of Pain (London, England)|June 3, 2017
Painful decisions: How classifying sensations can change the experience of painM A van der Meulen, F Anton, S Petersen
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|November 1, 1995
Perspectives of identity by descent (IBD) mapping in founder populationsG J Te Meerman, M A Van der Meulen, L A Sandkuijl
Journal of Medical Genetics|February 1, 1995
Recurrence risk for germinal mosaics revisitedM A van der Meulen, M J van der Meulen, G J te Meerman
American Journal of Human Genetics|December 1, 1993
Linkage analysis by two-dimensional DNA typingG J te Meerman, E Mullaart, M A van der Meulen, et al.
Human Genetics|September 1, 1996
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 populationsH G de Vries, M A van der Meulen, R Rozen, et al.
Human Genetics|December 1, 1995
Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type IC C Verschuuren-Bemelmans, E R Brunt, M Burton, et al.
European Journal of Cancer (Oxford, England : 1990)|June 9, 1998
A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testingA Dørum, P Møller, E J Kamsteeg, et al.
Pageof 1