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Gilliam, T. Conrad
One or more keywords matched the following items that are connected to Gilliam, T. Conrad
Item TypeName
Concept Chromosome Banding
Concept Chromosomes, Human, Pair 2
Concept Chromosomes, Human, Pair 6
Concept Chromosomes, Human, Pair 8
Concept Chromosomes, Human, Pair 1
Concept Chromosomes, Human, Pair 15
Concept Chromosomes, Human, Pair 21
Concept Chromosomes, Human, Pair 12
Concept Chromosomes, Human, Pair 14
Concept Chromosome Deletion
Concept Chromosome Mapping
Concept Chromosomes, Human, Pair 13
Concept Chromosomes, Human, Pair 4
Concept Chromosomes, Human, Pair 5
Concept Chromosomes, Human, Pair 7
Concept Chromosomes, Human, Pair 20
Concept Chromosomes, Human, Pair 10
Concept Chromosomes, Human, Pair 17
Concept Chromosomes, Human, Pair 19
Concept Chromosomes, Human, Pair 9
Concept Chromosome Inversion
Concept Chromosome Disorders
Concept Chromosome Aberrations
Concept Chromosomes, Human, Pair 16
Concept Chromosomes, Human, Pair 18
Concept X Chromosome
Concept Chromosome Breakage
Concept Physical Chromosome Mapping
Academic Article High resolution physical map of the region surrounding the spinal muscular atrophy gene.
Academic Article Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8p.
Academic Article High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p.
Academic Article No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees.
Academic Article Identification and localization of microsatellite markers covering human chromosome 18.
Academic Article Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3.
Academic Article Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12.
Academic Article Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris.
Academic Article A genomewide screen of 345 families for autism-susceptibility loci.
Academic Article Evidence for sex-specific risk alleles in autism spectrum disorder.
Academic Article Gene expression differences in mice divergently selected for methamphetamine sensitivity.
Academic Article Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Academic Article Genetic architecture of fear conditioning in chromosome substitution strains: relationship to measures of innate (unlearned) anxiety-like behavior.
Academic Article Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata.
Academic Article Recurrent 16p11.2 microdeletions in autism.
Academic Article Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
Academic Article Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network.
Academic Article Dinucleotide repeat polymorphism at the D19S206 locus.
Academic Article Dinucleotide repeat polymorphism at the D4S251 locus.
Academic Article Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p.
Academic Article Molecular and statistical approaches to the detection and correction of errors in genotype databases.
Academic Article Bipolar disorder and linkage to Xq28.
Academic Article Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy.
Academic Article Report of the first international workshop on human chromosome 18 mapping.
Academic Article Genetic alterations of microsatellites on chromosome 18 in human breast carcinoma.
Academic Article A microsatellite genetic linkage map of human chromosome 13.
Academic Article Dinucleotide repeat polymorphism at the D1S182 locus.
Academic Article A microsatellite genetic linkage map of human chromosome 18.
Academic Article A genomewide screen for autism susceptibility loci.
Academic Article Large-scale copy number polymorphism in the human genome.
Academic Article Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21.
Academic Article Perils of gene mapping with microsatellite markers.
Academic Article Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia.
Academic Article Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.
Academic Article Mapping psychiatric disease genes: impact of new molecular strategies.
Academic Article DNA markers for nervous system diseases.
Academic Article Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene.
Academic Article Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy.
Academic Article Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1B.
Academic Article An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy.
Academic Article A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions.
Academic Article Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues.
Academic Article Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24.
Academic Article The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8.
Academic Article Positional cloning and characterisation of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardation.
Academic Article Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs.
Academic Article Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13.
Academic Article Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions.
Academic Article Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.
Academic Article Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24.
Academic Article Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome.
Academic Article Linkage analysis of psychosis in bipolar pedigrees suggests novel putative loci for bipolar disorder and shared susceptibility with schizophrenia.
Academic Article Genomewide linkage analysis of celiac disease in Finnish families.
Academic Article A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22.
Academic Article Mapping complex traits in diseases of the hair and skin.
Academic Article Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21.
Academic Article Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q.
Academic Article Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosis.
Academic Article The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers.
Academic Article Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4.
Academic Article Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere.
Academic Article Molecular genetics of human chromosome 4.
Academic Article Molecular genetics of Huntington's disease.
Academic Article Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder.
Academic Article A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene.
Academic Article Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q.
Academic Article Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.
Academic Article A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus.
Academic Article A genetic linkage map of the chromosome 4 short arm.
Academic Article A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease gene.
Academic Article Isolation of polymorphic DNA fragments from human chromosome 4.
Academic Article A human anonymous low copy number clone, 4c11 (D6S4), localized to 6p12-6p21, detects 2 RFLPs, one of which is moderately polymorphic.
Academic Article Pairwise linkage analysis of 11 loci on human chromosome 4.
Academic Article Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q.
Academic Article Results of a genome-wide genetic screen for panic disorder.
Academic Article Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy.
Academic Article Is the spinal muscular atrophy gene found?
Academic Article Progress toward cloning of the gene responsible for childhood spinal muscular atrophy.
Academic Article A DNA segment encoding two genes very tightly linked to Huntington's disease.
Academic Article Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28.
Academic Article Genetic analysis of childhood-onset spinal muscular atrophy.
Academic Article Genetic mapping of "Lubag" (X-linked dystonia-parkinsonism) in a Filipino kindred to the pericentromeric region of the X chromosome.
Academic Article Genetic homogeneity between acute and chronic forms of spinal muscular atrophy.
Academic Article Physical mapping, linkage analysis of a putative schizophrenia locus on chromosome 5q.
Academic Article Chromosome jumping from D4S10 (G8) toward the Huntington disease gene.
Academic Article Molecular genetic strategies to investigate Huntington's disease.
Academic Article Genetic mapping of chronic childhood-onset Spinal Muscular Atrophy to Chromosome 5q11.2-13.3
Search Criteria
  • Chromosomes Human Pair 2