1996
Searching for major genes for schizophrenia
Kidd K. Searching for major genes for schizophrenia. 1996, 539-556. DOI: 10.1017/cbo9780511664052.030.ChaptersGenetics of schizophreniaSubstantial genetic componentGenetic variationSingle locusMajor geneRelevant genesGenetic studiesGenesGenetic componentEtiology of schizophreniaGenetic hypothesisGeneticsGenetic transmissionGenetic factorsGenetic influencesClasses of relativesLociApparent discriminationRelativesMatthysse
1989
The β subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies
Wu J, Giuffra L, Goodfellow P, Myers S, Carson N, Anderson L, Hoyle L, Simpson N, Kidd K. The β subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies. Human Genetics 1989, 83: 383-390. PMID: 2572537, DOI: 10.1007/bf00291386.Peer-Reviewed Original ResearchMeSH KeywordsChromosome MappingChromosomes, Human, Pair 1Chromosomes, Human, Pair 10Chromosomes, Human, Pair 17Chromosomes, Human, Pair 21DNADNA ProbesDNA, NeoplasmFemaleGenetic LinkageGenetic MarkersHaplotypesHumansMaleMultiple Endocrine NeoplasiaPolymorphism, Restriction Fragment LengthReceptors, FibronectinReceptors, ImmunologicConceptsRestriction fragment length polymorphismHuman fibronectin receptorCDNA clonesFragment length polymorphismLinkage analysisDNA restriction fragment length polymorphismsMultiple restriction fragment length polymorphismsPolymorphism information content (PIC) valuesFibronectin receptorHighest polymorphism information content valuePartial cDNA cloneInformation content valuesLength polymorphismLinkage studiesPairwise linkage analysisSouthern blot analysisTypes of polymorphismsChromosome 10 markersGenomic clonesPericentromeric regionTransmembrane proteinDNA markersGenetic linkage studiesDNA sequencesSingle locus
1982
Recombinant DNA approach to neurogenetic disorders
Housman D, Kidd K, Gusella J. Recombinant DNA approach to neurogenetic disorders. Trends In Neurosciences 1982, 5: 320-323. DOI: 10.1016/0166-2236(82)90192-8.Peer-Reviewed Original ResearchHuman neurogenetic disordersRecombinant DNA techniquesDNA techniquesGenetic linkage methodsRecombinant DNA approachesCharacterization of sequencesNeurogenetic disordersSingle locusDNA sequencesDNA approachAbnormal phenotypeDNA copiesNeurological phenotypeOrganismsPolypeptidePhenotypeHuntington's diseaseSequence