| Item Type | Name |
|
Concept
|
Chromosome Banding
|
|
Concept
|
Chromosomes, Human, Pair 2
|
|
Concept
|
Chromosomes, Human, Pair 6
|
|
Concept
|
Chromosomes, Human, Pair 8
|
|
Concept
|
Chromosomes, Bacterial
|
|
Concept
|
Chromosomes, Human, Pair 1
|
|
Concept
|
Chromosomes, Human, Pair 15
|
|
Concept
|
Chromosomes, Human, Pair 21
|
|
Concept
|
Chromosomes, Human, 4-5
|
|
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
|
Chromosomes, Artificial, Bacterial
|
|
Concept
|
Chromosomes, Mammalian
|
|
Concept
|
Chromosomes, Artificial, Yeast
|
|
Concept
|
Chromosome Disorders
|
|
Concept
|
Chromosome Aberrations
|
|
Concept
|
Chromosomes, Human
|
|
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
|