Annals of Human Genetics · 1996 · 26 citations · 10 references
Life SciencesGeneticsMolecular GeneticsCytogeneticsHuman GeneticsMedical GeneticsChromosomal AbnormalitiesGene MappingGenetic DisordersGenetic LinkageGenetic SyndromesLinkage AnalysisAutosomal Dominant InheritanceGenetic Linkage AnalysisGenetic Linkage MappingGenetic Linkage MapsLod Score AnalysisMelanin AccumulationMelanin ProductionPigmentation
Peutz-Jeghers' syndrome (PJS) is a disease with autosomal dominant inheritance, which is characterised by gastrointestinal hamartomata and characteristic melanin pigmentation. Three candidate sites for a PJS locus have recently been proposed, chromosomes 1p31-p32, 6q25 and 6p11-cen. At the first of these sites, a multipoint LOD score of 4.00 had been found, strongly suggesting genetic linkage to PJS. The last two candidate sites were suggested by the chromosomal breakpoints of a patient with an inv(6) and PJS. We have analysed up to 34 families in order to test each of the three candidate sites for linkage to PJS. No evidence was found in support of a Peutz-Jeghers' syndrome locus on chromosome 1p31-p32. The candidate region on 6q25 was also excluded. The region close to the centromere of chromosome 6 has not been excluded and there is some evidence of linkage to a marker near 6cen, although genetic heterogeneity in PJS must be proposed to account for a gene at this site.
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Handbook of human genetic linkage
Elizabeth M. Petty · Trends in Endocrinology and Metabolism · 1995 · 565 citations
Life Sciences, Biology, Genetics +11
The affected-pedigree-member method of linkage analysis.
Daniel E. Weeks, Kenneth Lange · PubMed · 1988 · 492 citations