Genetic linkage analysis

HLA-association of serum levels of natural antibodies

Genetics / Immunology / Immune response / Polymorphism / Family / Regulation / Molecular / Molecular Immunology / Humans / Child / MHC / HLA / Adaptive Immunity / Female / Male / Genetic linkage analysis / Adult / Major histocompatibility complex / Heat Shock Proteins / Heat Shock Protein / Family Study / Citrate Synthase / Autoantibodies / Chondroitin Sulphate / Regulation / Molecular / Molecular Immunology / Humans / Child / MHC / HLA / Adaptive Immunity / Female / Male / Genetic linkage analysis / Adult / Major histocompatibility complex / Heat Shock Proteins / Heat Shock Protein / Family Study / Citrate Synthase / Autoantibodies / Chondroitin Sulphate

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HLA-association of serum levels of natural antibodies

Genetics / Immunology / Immune response / Polymorphism / Family / Molecular / Molecular Immunology / Humans / Child / Adaptive Immunity / Female / Male / Genetic linkage analysis / Adult / Major histocompatibility complex / Heat Shock Protein / Family Study / Citrate Synthase / Autoantibodies / Chondroitin Sulphate / Molecular / Molecular Immunology / Humans / Child / Adaptive Immunity / Female / Male / Genetic linkage analysis / Adult / Major histocompatibility complex / Heat Shock Protein / Family Study / Citrate Synthase / Autoantibodies / Chondroitin Sulphate

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HLA-association of serum levels of natural antibodies

Genetics / Immunology / Immune response / Polymorphism / Family / Molecular / Molecular Immunology / Humans / Child / Adaptive Immunity / Female / Male / Genetic linkage analysis / Adult / Major histocompatibility complex / Heat Shock Protein / Family Study / Citrate Synthase / Autoantibodies / Chondroitin Sulphate / Molecular / Molecular Immunology / Humans / Child / Adaptive Immunity / Female / Male / Genetic linkage analysis / Adult / Major histocompatibility complex / Heat Shock Protein / Family Study / Citrate Synthase / Autoantibodies / Chondroitin Sulphate

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Familial nephrotic syndrome: Clinical spectrum and linkage to chromosome 19q13

Genetics / Adolescent / Humans / Child / Kidney / Female / Renal failure / Male / Polymerase Chain Reaction / Infant / Pedigree / Genetic linkage analysis / Clinical Sciences / Spectrum / Genomic DNA / Adult / Disease Progression / Renal biopsy / Clinical Presentation / Area of Interest / Linkage Analysis / Nephrotic syndrome / Focal Segmental Glomerulosclerosis / Female / Renal failure / Male / Polymerase Chain Reaction / Infant / Pedigree / Genetic linkage analysis / Clinical Sciences / Spectrum / Genomic DNA / Adult / Disease Progression / Renal biopsy / Clinical Presentation / Area of Interest / Linkage Analysis / Nephrotic syndrome / Focal Segmental Glomerulosclerosis

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Presymptomatic diagnosis of myotonic dystrophy

Medical Genetics / Biological Sciences / DNA / Humans / Female / Male / Polymerase Chain Reaction / Myotonic Dystrophy / Pedigree / Genetic linkage analysis / Aged / Middle Aged / Adult / Clinical Data / Base Sequence / Prospective Study / Medical / Male / Polymerase Chain Reaction / Myotonic Dystrophy / Pedigree / Genetic linkage analysis / Aged / Middle Aged / Adult / Clinical Data / Base Sequence / Prospective Study / Medical

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Genetics of Photosensitivity (Photoparoxysmal Response): A Review

Genetics / Humans / Animals / Photosensitivity / Phenotype / Genetic linkage analysis / Epilepsia / Clinical Sciences / Neurosciences / Genetic linkage analysis / Epilepsia / Clinical Sciences / Neurosciences

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Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference

Genetics / Cognitive Science / Dementia / Magnetic Resonance Imaging / Neuropathology / Molecular Genetics / Poland / Movement disorders / Genetic counseling / Temporal Lobe / Brain / Humans / Mutation / Female / Male / Differential Diagnosis / Electromyography / Life Expectancy / Pedigree / Genetic linkage analysis / Clinical Sciences / North America / Middle Aged / Cognitive impairment / Adult / Frontotemporal Dementia / X ray Computed Tomography / Protein Binding / Psychomotor Disorders / Neurosciences / Frontal Lobe / Parkinson Disease / Cognition disorders / Molecular Genetics / Poland / Movement disorders / Genetic counseling / Temporal Lobe / Brain / Humans / Mutation / Female / Male / Differential Diagnosis / Electromyography / Life Expectancy / Pedigree / Genetic linkage analysis / Clinical Sciences / North America / Middle Aged / Cognitive impairment / Adult / Frontotemporal Dementia / X ray Computed Tomography / Protein Binding / Psychomotor Disorders / Neurosciences / Frontal Lobe / Parkinson Disease / Cognition disorders

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Tau is a candidate gene for chromosome 17 frontotemporal dementia

Dementia / Temporal Lobe / Humans / Female / Male / Pedigree / Genetic linkage analysis / Clinical Sciences / Family Health / Frontotemporal Dementia / Annals / Neurosciences / Frontal Lobe / Pedigree / Genetic linkage analysis / Clinical Sciences / Family Health / Frontotemporal Dementia / Annals / Neurosciences / Frontal Lobe

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Comparison of Strategies to Detect Epistasis from eQTL Data

Genetics / Computational Biology / Gene expression / Multidisciplinary / Saccharomyces cerevisiae / Humans / PLoS one / Genetic linkage analysis / Quantitative Trait Loci / False discovery rate / Human Disease / Complex Traits / Humans / PLoS one / Genetic linkage analysis / Quantitative Trait Loci / False discovery rate / Human Disease / Complex Traits

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Frontotemporal Dementia Linked to Chromosome 3

Genetics / Cognitive Science / Dementia / Molecular Genetics / Denmark / Brain / Humans / Male / Phenotype / Genetic linkage analysis / Clinical Sciences / Frontotemporal Dementia / Neurosciences / Brain / Humans / Male / Phenotype / Genetic linkage analysis / Clinical Sciences / Frontotemporal Dementia / Neurosciences

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A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3

Survival Analysis / Probability / Biological Sciences / Humans / Child / Female / Male / Pedigree / Genetic linkage analysis / Introns / Survival Rate / Age Factors / Genetic Recombination / Troponin / Tropomyosin / Base Sequence / Hypertrophic Cardiomyopathy / Genetic Markers / Troponin I / Contractile Proteins / Female / Male / Pedigree / Genetic linkage analysis / Introns / Survival Rate / Age Factors / Genetic Recombination / Troponin / Tropomyosin / Base Sequence / Hypertrophic Cardiomyopathy / Genetic Markers / Troponin I / Contractile Proteins

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Three autosomal dominant corneal dystrophies map to chromosome 5q

Amyloid / Italy / Biological Sciences / Humans / United States / Female / Male / Pedigree / Genetic linkage analysis / Genetic Markers / Female / Male / Pedigree / Genetic linkage analysis / Genetic Markers

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CAMOS, a nonprogressive, autosomal recessive, congenital cerebellar ataxia, is caused by a mutant zinc-finger protein, ZNF592

Genetics / Lebanon / Intellectual Disability / Mental Retardation / Humans / C2H2 zinc fingers / Cerebellar ataxia / Genetic linkage analysis / European / Zinc Finger / Family Health / DNA binding / Disease Progression / Amino Acid Profile / Amino Acid Sequence / Autosomal Recessive / DNA binding proteins / Genetic Markers / Gene Expression Regulation / Zinc Finger Protein / C2H2 zinc fingers / Cerebellar ataxia / Genetic linkage analysis / European / Zinc Finger / Family Health / DNA binding / Disease Progression / Amino Acid Profile / Amino Acid Sequence / Autosomal Recessive / DNA binding proteins / Genetic Markers / Gene Expression Regulation / Zinc Finger Protein

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Prevalence of retinitis pigmentosa in Slovenia

Genetics / Adolescent / Humans / Child / Retinitis pigmentosa / Sex ratio / Female / Clinical Genetics / Male / Infant / Slovenia / Genetic linkage analysis / Clinical Sciences / Newborn Infant / Aged / Prevalence / Middle Aged / Adult / X chromosome / Sex ratio / Female / Clinical Genetics / Male / Infant / Slovenia / Genetic linkage analysis / Clinical Sciences / Newborn Infant / Aged / Prevalence / Middle Aged / Adult / X chromosome

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Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17

Cognitive Science / Dementia / Humans / Female / Male / Differential Diagnosis / Pedigree / Genetic linkage analysis / Clinical Sciences / Middle Aged / Adult / Prion disease / Frontotemporal Dementia / Age at Onset / Differential Diagnosis / Pedigree / Genetic linkage analysis / Clinical Sciences / Middle Aged / Adult / Prion disease / Frontotemporal Dementia / Age at Onset

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Tau is a candidate gene for chromosome 17 frontotemporal dementia

Dementia / Temporal Lobe / Humans / Female / Male / Pedigree / Genetic linkage analysis / Clinical Sciences / Family Health / Frontotemporal Dementia / Annals / Neurosciences / Frontal Lobe / Pedigree / Genetic linkage analysis / Clinical Sciences / Family Health / Frontotemporal Dementia / Annals / Neurosciences / Frontal Lobe

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