1996
Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization
Haaf T, Sirugo G, Kidd K, Ward D. Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization. Nature Genetics 1996, 12: 183-185. PMID: 8563757, DOI: 10.1038/ng0296-183.Peer-Reviewed Original ResearchConceptsLong trinucleotide repeatsChromosomal localizationTrinucleotide repeatsHuman genomeNormal human genomeSitu hybridizationDifferent genetic diseasesUnstable trinucleotide repeatsChromosomal distributionTrinucleotide microsatellitesLarge repeatsAGG repeatsCCG repeatsRepeatsGenetic diseasesRepeat lociLarge CTG expansionsGenomeCTG expansionHybridizationPathological significanceMyotonic dystrophyMicrosatellitesLocalizationLoci
1993
A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus
Lichter J, Wu J, Brooks-Wilson A, Difillipantonio M, Brewster S, Ward D, Goodfellow P, Kidd K. A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus. Human Genetics 1993, 90: 516-520. PMID: 8094065, DOI: 10.1007/bf00217451.Peer-Reviewed Original ResearchMeSH KeywordsAnimalsBase SequenceChromosome MappingChromosomes, FungalChromosomes, Human, Pair 10Cloning, MolecularCricetinaeDeoxyribonuclease EcoRIDNADNA ProbesFemaleGene FrequencyGene LibraryGenetic LinkageGenetic MarkersGenome, HumanHumansHybrid CellsIn Situ Hybridization, FluorescenceLod ScoreMaleMolecular Sequence DataMultiple Endocrine NeoplasiaPedigreePolymorphism, GeneticPolymorphism, Restriction Fragment LengthSequence Analysis, DNA
1992
Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10
Miller D, Dill F, Lichter J, Kidd K, Goodfellow P. Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10. Genomics 1992, 13: 601-606. PMID: 1353474, DOI: 10.1016/0888-7543(92)90130-k.Peer-Reviewed Original ResearchExclusion of Linkage Between the Serotonin2 Receptor and Schizophrenia in a Large Swedish Kindred
Hallmayer J, Kennedy J, Wetterberg L, Sjögren B, Kidd K, Cavalli-Sforza L. Exclusion of Linkage Between the Serotonin2 Receptor and Schizophrenia in a Large Swedish Kindred. JAMA Psychiatry 1992, 49: 216-219. PMID: 1348924, DOI: 10.1001/archpsyc.1992.01820030048006.Peer-Reviewed Original ResearchPresymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A
Lichter J, Wu J, Genel M, Flynn S, Pakstis A, Kidd J, Kidd K. Presymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A. The Journal Of Clinical Endocrinology & Metabolism 1992, 74: 368-373. PMID: 1346145, DOI: 10.1210/jcem.74.2.1346145.Peer-Reviewed Original Research
1991
Two RFLPs at the HOX2G locus
Ogura T, Castiglione C, Pakstis A, Kidd K. Two RFLPs at the HOX2G locus. Nucleic Acids Research 1991, 19: 1716-1716. PMID: 1674132, PMCID: PMC333946, DOI: 10.1093/nar/19.7.1716-a.Peer-Reviewed Original ResearchAn Mspl polymorphism for the HOX2F gene
Ogura T, Castiglione C, Pakstis A, Kidd K. An Mspl polymorphism for the HOX2F gene. Nucleic Acids Research 1991, 19: 1716-1716. PMID: 1709280, PMCID: PMC333945, DOI: 10.1093/nar/19.7.1716.Peer-Reviewed Original Research
1990
A refined linkage map for DNA markers around the pericentromeric region of chromosome 10
Wu J, Myers S, Carson N, Kidd J, Anderson L, Castiglione C, Hoyle L, Lichter J, Sukhatme V, Simpson N, Kidd K. A refined linkage map for DNA markers around the pericentromeric region of chromosome 10. Genomics 1990, 8: 461-468. PMID: 1981049, DOI: 10.1016/0888-7543(90)90032-p.Peer-Reviewed Original ResearchThe Na+/H+ antiporter: a “melt” polymorphism allows regional mapping to the short arm of chromosome 1
Dudley C, Giuffra L, Tippett P, Kidd K, Reeders S. The Na+/H+ antiporter: a “melt” polymorphism allows regional mapping to the short arm of chromosome 1. Human Genetics 1990, 86: 79-83. PMID: 1979310, DOI: 10.1007/bf00205179.Peer-Reviewed Original Research
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
1988
The ornithine aminotransferase (OAT) locus is linked and distal to D10S20 on the long arm of chromosome 10
Wu J, Ramesh V, Kidd J, Castiglione C, Myers S, Carson N, Anderson L, Gusella J, Simpson N, Kidd K. The ornithine aminotransferase (OAT) locus is linked and distal to D10S20 on the long arm of chromosome 10. Cytogenetic And Genome Research 1988, 48: 126-127. PMID: 3197452, DOI: 10.1159/000132606.Peer-Reviewed Original Research