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Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs.
Trait components provide tools to dissect the genetic susceptibility of migraine.
A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers.
Consistently replicating locus linked to migraine on 10q22-q23.
Sweet taste preferences are partly genetically determined: identification of a trait locus on chromosome 16.
Chromosome 19p13 loci in Finnish migraine with aura families.
Fine mapping of the multiple sclerosis susceptibility locus on 5p14-p12.
Combined genome scans for body stature in 6,602 European twins: evidence for common Caucasian loci.
Association of the timing of puberty with a chromosome 2 locus.
Early-onset osteoarthritis linked to the type II procollagen gene. Detailed clinical phenotype and further analyses of the gene.
Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups.
Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2.
Presymptomatic DNA and MRI diagnosis of neurofibromatosis 2 with mild clinical course in an extended pedigree.
Novel splice site CACNA1A mutation causing episodic ataxia type 2.
A susceptibility locus for migraine with aura, on chromosome 4q24.