Item Type | Name |
Concept
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Chromosomes, Human, Pair 2
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Concept
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Chromosomes, Human, Pair 6
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Concept
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Chromosomes, Human, Pair 8
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Concept
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Chromosomes, Human, Pair 1
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Concept
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Chromosomes, Human, Pair 15
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Concept
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Chromosomes, Human, Pair 21
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Concept
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Chromosomes, Human, 4-5
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Concept
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Chromosomes, Human, Pair 12
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Concept
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Chromosomes, Human, Pair 14
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Concept
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Chromosomes, Human, Pair 13
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Concept
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Chromosomes, Human, Pair 4
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Concept
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Chromosomes, Human, Pair 5
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Concept
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Chromosomes, Human, Pair 7
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Concept
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Chromosomes, Human, Pair 20
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Concept
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Chromosomes, Human, Pair 10
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Concept
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Chromosomes, Human, Pair 17
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Concept
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Chromosomes, Human, Pair 19
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Concept
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Chromosomes, Human, Pair 9
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Concept
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Chromosomes, Human
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Concept
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Chromosomes, Human, Pair 16
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Concept
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Chromosomes, Human, Pair 18
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Academic Article
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High resolution physical map of the region surrounding the spinal muscular atrophy gene.
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Academic Article
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Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8p.
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Academic Article
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High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p.
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Academic Article
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No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees.
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Academic Article
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Identification and localization of microsatellite markers covering human chromosome 18.
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Academic Article
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Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3.
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Academic Article
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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.
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Academic Article
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Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris.
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Academic Article
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Evidence for sex-specific risk alleles in autism spectrum disorder.
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Academic Article
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Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata.
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Academic Article
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Recurrent 16p11.2 microdeletions in autism.
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Academic Article
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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
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Academic Article
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Dinucleotide repeat polymorphism at the D19S206 locus.
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Academic Article
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Dinucleotide repeat polymorphism at the D4S251 locus.
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Academic Article
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Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p.
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Academic Article
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Molecular and statistical approaches to the detection and correction of errors in genotype databases.
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Academic Article
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Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy.
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Academic Article
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Report of the first international workshop on human chromosome 18 mapping.
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Academic Article
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Genetic alterations of microsatellites on chromosome 18 in human breast carcinoma.
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Academic Article
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A microsatellite genetic linkage map of human chromosome 13.
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Academic Article
|
Dinucleotide repeat polymorphism at the D1S182 locus.
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Academic Article
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A microsatellite genetic linkage map of human chromosome 18.
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Academic Article
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A genomewide screen for autism susceptibility loci.
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Academic Article
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Large-scale copy number polymorphism in the human genome.
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Academic Article
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Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21.
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Academic Article
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Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia.
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Academic Article
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Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.
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Academic Article
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Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene.
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Academic Article
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Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy.
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Academic Article
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Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1B.
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Academic Article
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An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy.
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Academic Article
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Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24.
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Academic Article
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Positional cloning and characterisation of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardation.
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Academic Article
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Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs.
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Academic Article
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Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13.
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Academic Article
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Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.
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Academic Article
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Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24.
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Academic Article
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Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome.
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Academic Article
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Linkage analysis of psychosis in bipolar pedigrees suggests novel putative loci for bipolar disorder and shared susceptibility with schizophrenia.
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Academic Article
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Genomewide linkage analysis of celiac disease in Finnish families.
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Academic Article
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A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22.
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Academic Article
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Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21.
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Academic Article
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Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q.
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Academic Article
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Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosis.
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Academic Article
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The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers.
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Academic Article
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Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4.
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Academic Article
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Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere.
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Academic Article
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Molecular genetics of human chromosome 4.
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Academic Article
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Molecular genetics of Huntington's disease.
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Academic Article
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A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene.
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Academic Article
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Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q.
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Academic Article
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Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.
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Academic Article
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A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus.
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Academic Article
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A genetic linkage map of the chromosome 4 short arm.
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Academic Article
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A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease gene.
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Academic Article
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Isolation of polymorphic DNA fragments from human chromosome 4.
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Academic Article
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A human anonymous low copy number clone, 4c11 (D6S4), localized to 6p12-6p21, detects 2 RFLPs, one of which is moderately polymorphic.
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Academic Article
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Pairwise linkage analysis of 11 loci on human chromosome 4.
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Academic Article
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Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q.
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Academic Article
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Results of a genome-wide genetic screen for panic disorder.
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Academic Article
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Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy.
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Academic Article
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Is the spinal muscular atrophy gene found?
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Academic Article
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A DNA segment encoding two genes very tightly linked to Huntington's disease.
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Academic Article
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Genetic analysis of childhood-onset spinal muscular atrophy.
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Academic Article
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Genetic homogeneity between acute and chronic forms of spinal muscular atrophy.
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Academic Article
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Physical mapping, linkage analysis of a putative schizophrenia locus on chromosome 5q.
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Academic Article
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Chromosome jumping from D4S10 (G8) toward the Huntington disease gene.
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Academic Article
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Molecular genetic strategies to investigate Huntington's disease.
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