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Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in Finns
GENOME RESEARCH
Experimentally-derived haplotypes substantially increase the efficiency oflinkage disequilibrium studies
NATURE GENETICS
Lod scores for gene mapping in the presence of marker map uncertainty
GENETIC EPIDEMIOLOGY
Leber's hereditary optic neuropathy mitochondrial DNA mutations in normal-tension glaucoma
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
Examination of genetic linkage of chromosome 15 to schizophrenia in a large veterans affairs cooperative study sample
AMERICAN JOURNAL OF MEDICAL GENETICS
The peroxisome poliferator-activated receptor-gamma 2 Pro12Ala variant - Association with type 2 diabetes and trait differences
DIABETES
A look at linkage disequilibrium
NATURE GENETICS
Effect of fortified antibiotic solutions on corneal epithelial wound healing
CORNEA
Early aqueous humor analysis in patients with human ocular toxoplasmosis
JOURNAL OF CLINICAL MICROBIOLOGY
The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes
AMERICAN JOURNAL OF HUMAN GENETICS
The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci
AMERICAN JOURNAL OF HUMAN GENETICS
Improved inference of relationship for pairs of individuals
AMERICAN JOURNAL OF HUMAN GENETICS
A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data
AMERICAN JOURNAL OF HUMAN GENETICS
Influences of methylcellulose on corneal epithelial wound healing
JOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICS
Loss of information due to ambiguous haplotyping of SNPs
NATURE GENETICS
Eyelid, conjunctival, and corneal findings in sleep apnea syndrome
OPHTHALMOLOGY
Type 2 diabetes: Evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
The W64R variant of the beta(3)-adrenergic receptor is not associated withType II diabetes or obesity in a large Finnish sample
DIABETOLOGIA
Point and interval estimates of marker location in radiation hybrid mapping
AMERICAN JOURNAL OF HUMAN GENETICS
Familiality of quantitative metabolic traits in Finnish families with non-insulin-dependent diabetes mellitus
HUMAN HEREDITY
NOVEL TRABECULAR MESHWORK INDUCIBLE GLUCOCORTICOID RESPONSE MUTATION IN AN 8-GENERATION JUVENILE-ONSET PRIMARY OPEN-ANGLE GLAUCOMA PEDIGREE
Ophthalmology (Rochester, Minn.)
MAPPING GENES FOR NIDDM - DESIGN OF THE FINLAND UNITED-STATES INVESTIGATION OF NIDDM GENETICS (FUSION) STUDY
Diabetes care
EXPERIMENTAL OCULAR TOXOPLASMOSIS IN NAIVE AND PRIMED RABBITS
Ophthalmologica
A LARGE-SAMPLE OF FINNISH DIABETIC SIB-PAIRS REVEALS NO EVIDENCE FOR A NON-INSULIN-DEPENDENT DIABETES-MELLITUS SUSCEPTIBILITY LOCUS AT 2QTER
The Journal of clinical investigation
LINKAGE ANALYSIS OF NIDDM-RELATED QUANTITATIVE TRAITS IN THE FUSION STUDY - COMPARISON WITH NIDDM LINKAGE RESULTS FOR CHROMOSOME-20
Diabetes
AUTOSOMAL-DOMINANT NANOPHTHALMOS (NNO1) WITH HIGH HYPEROPIA AND ANGLE-CLOSURE GLAUCOMA MAPS TO CHROMOSOME-11
American journal of human genetics
FINE LOCALIZATION OF THE NIJMEGEN BREAKAGE SYNDROME GENE TO 8Q21 - EVIDENCE FOR A COMMON FOUNDER HAPLOTYPE
American journal of human genetics
GENETIC ASSOCIATION MAPPING BASED ON DISCORDANT SIB PAIRS - THE DISCORDANT-ALLELES TEST
American journal of human genetics
METHODS FOR PRECISE SIZING, AUTOMATED BINNING OF ALLELES, AND REDUCTION OF ERROR RATES IN LARGE-SCALE GENOTYPING USING FLUORESCENTLY LABELED DINUCLEOTIDE MARKERS
PCR methods and applications
LOW-RATE SHEDDING OF HSV-1 DNA, BUT NOT OF INFECTIOUS VIRUS FROM HUMAN DONOR CORNEAE INTO CULTURE MEDIA
Journal of medical virology
PROBABLE EXCLUSION OF GLC1B AS A CANDIDATE LOCUS IN 2 MIDDLE-AGE-ONSET PRIMARY OPEN-ANGLE GLAUCOMA FAMILIES
Investigative ophthalmology & visual science
MULTIPOINT LINKAGE ANALYSIS OF NIDDM IN 534 FINNISH FAMILIES IN THE FUSION STUDY
Diabetologia
MULTIPOINT LINKAGE ANALYSIS OF NIDDM IN 534 FINNISH FAMILIES IN THE FUSION STUDY
Diabetes
COSEGREGATION OF OPEN-ANGLE GLAUCOMA AND THE NAIL-PATELLA SYNDROME
American journal of ophthalmology
JUVENILE GLAUCOMA LINKED TO THE GLC1A GENE ON CHROMOSOME 1Q IN A PANAMANIAN FAMILY
American journal of ophthalmology
GLAUCOMA AND NAIL-PATELLA SYNDROME (NPS) CO-SEGREGATE - ONE GENE OR 2
American journal of human genetics
MAPPING NIJMEGEN-BREAKAGE-SYNDROME TO 8Q21 AND CONSTRUCTION OF A RADIATION HYBRID MAP OF THE D8S1757-D8S506 REGION
American journal of human genetics
A BAYESIAN-APPROACH TO RADIATION HYBRID MAPPING
American journal of human genetics
A TRANSMISSION DISEQUILIBRIUM TEST THAT USES BOTH AFFECTED AND UNAFFECTED OFFSPRING/
American journal of human genetics
SOFTWARE FOR DETERMINING MOST LIKELY RELATIONSHIPS IN RELATIVE PAIRS
American journal of human genetics
THE FUSION (FINLAND UNITED-STATES INVESTIGATION OF NIDDM GENETICS) STUDY
American journal of human genetics
CONFIRMATION OF LINKAGE RESULTS IN AFFECTED-SIB-PAIR LINKAGE ANALYSISFOR COMPLEX GENETIC-TRAITS
American journal of human genetics
FAMILY-BASED TESTS FOR ASSOCIATION USING DISCORDANT SIB PAIRS
American journal of human genetics
FAMILIALITY OF MINIMAL MODEL-DERIVED QUANTITATIVE METABOLIC TRAITS INA FINNISH COHORT
American journal of human genetics
ACCURATE INFERENCE OF RELATIONSHIPS IN SIB-PAIR LINKAGE STUDIES
American journal of human genetics
RESTRICTED APPLICABILITY OF THE POLYMERASE CHAIN-REACTION FOR THE DIAGNOSIS OF OCULAR TOXOPLASMOSIS
German journal of ophthalmology
LOCALIZATION OF THE HOMOLOG OF A MOUSE CRANIOFACIAL MUTANT TO HUMAN-CHROMOSOME 18Q11 AND EVALUATION OF LINKAGE TO HUMAN CLP AND CPO
Genomics
AFFECTED-SIB-PAIR INTERVAL MAPPING AND EXCLUSION FOR COMPLEX GENETIC-TRAITS - SAMPLING CONSIDERATIONS
Genetic epidemiology
PROBABLE EXCLUSION OF GLC1A AS A CANDIDATE GLAUCOMA GENE IN A FAMILY WITH MIDDLE-AGE-ONSET PRIMARY OPEN-ANGLE GLAUCOMA
Ophthalmology
CLINICAL PHENOTYPE OF JUVENILE-ONSET PRIMARY OPEN-ANGLE GLAUCOMA LINKED TO CHROMOSOME 1Q
Ophthalmology
GENETICS OF MIDDLE-AGE ONSET PRIMARY OPEN-ANGLE GLAUCOMA
Investigative ophthalmology & visual science
VARICELLA-ZOSTER VIRUS IS THE MAIN PATHOGEN IN ATYPICAL NECROTIZING RETINOPATHIES IN AIDS PATIENTS
Vision research
FAMILIALITY OF QUANTITATIVE METABOLIC TRAITS IN A FINNISH POPULATION
Diabetologia
GENES FOR NIDDM IN THE HLA REGION ON CHROMOSOME-6 - THE FINLAND UNITED-STATES INVESTIGATION OF NIDDM GENETICS (FUSION)
Diabetes
THE BETA-3 ADRENERGIC-RECEPTOR CODON-64 VARIANT IS NOT ASSOCIATED WITH AGE-AT-DIAGNOSIS OF NIDDM NOR WITH OBESITY IN THE FUSION (FINNISH USINVESTIGATION OF NIDDM) STUDY
Diabetes
POLYMORPHISM OF ADHESION MOLECULE CD31 IS NOT A SIGNIFICANT RISK FACTOR FOR GRAFT-VERSUS-HOST DISEASE
Blood
IDENTIFYING MARKER TYPING INCOMPATIBILITIES IN LINKAGE ANALYSIS
American journal of human genetics
SELECTED LOCUS AND MULTIPLE PANEL MODELS FOR RADIATION HYBRID MAPPING
American journal of human genetics
LINKAGE STUDY OF BESTS VITELLIFORM MACULAR DYSTROPHY (VMD2) IN A LARGE NORTH-AMERICAN FAMILY
Human heredity
LOD SCORE CURVES FOR PHASE-UNKNOWN MATINGS
Human heredity
STATISTICAL-METHODS FOR POLYPLOID RADIATION HYBRID MAPPING
PCR methods and applications
EXPERIMENTAL-DESIGN AND ERROR-DETECTION FOR POLYPLOID RADIATION HYBRID MAPPING
PCR methods and applications
RECOMBINATION FRACTION ESTIMATE OF ZERO IN THE PRESENCE OF APPARENT RECOMBINANTS - EFFECTS OF INCOMPLETE PENETRANCE AND SPORADIC CASES
Genetic epidemiology
LOCALIZATION OF THE HUMAN HOMOLOG OF THE YEAST CELL-DIVISION-CONTROL-27 GENE (CDC27) PROXIMAL TO ITGB3 ON HUMAN-CHROMOSOME 17Q21.3
Somatic cell and molecular genetics
BESTS VITELLIFORM MACULAR DYSTROPHY (VMD2) - LOCALIZATION BETWEEN D11S903 D11S956 AND ROM1 AND LIKELY EXCLUSION OF ROM1 AS CANDIDATE GENE/
Investigative ophthalmology & visual science
JUVENILE RETINOSCHISIS (RS) - REFINED X-CHROMOSOME MAPPING
Investigative ophthalmology & visual science
IDENTIFICATION OF NON-HLA LOCI CONTRIBUTING TO GRAFT-VERSUS-HOST DISEASE
Blood
EXPERIMENTAL-DESIGN CONSIDERATIONS FOR WHOLE-GENOME RADIATION HYBRIDS
American journal of human genetics
STATISTICAL-METHODS FOR POLYPLOID RADIATION HYBRID MAPPING
American journal of human genetics
AFFECTED-SIB-PAIR LINKAGE AND EXCLUSION MAPPING - MULTIPOINT EXTENSION, STATISTICAL PROPERTIES, AND ROBUSTNESS
American journal of human genetics
RECOMBINATION FRACTION ESTIMATE OF ZERO IN THE PRESENCE OF APPARENT RECOMBINANTS - EFFECTS OF INCOMPLETE PENETRANCE AND SPORADIC CASES
American journal of human genetics
AN EVALUATION OF GENETIC-HETEROGENEITY IN 145 BREAST-CANCER OVARIAN-CANCER FAMILIES
American journal of human genetics
BREAST AND OVARIAN-CANCER INCIDENCE IN BRCAI-MUTATION CARRIERS
American journal of human genetics
REFINED GENETIC-MAPPING OF JUVENILE X-LINKED RETINOSCHISIS
Human heredity
A DISEASE LOCUS FOR HEREDITARY HEMORRHAGIC TELANGIECTASIA MAPS TO CHROMOSOME 9Q33-34
Nature genetics
INTEGRATED MAPPING ANALYSIS OF THE WERNER SYNDROME REGION OF CHROMOSOME-8
Genomics
LOCALIZATION OF THE GENE FOR ATP CITRATE LYASE (ACLY) DISTAL TO GASTRIN (GAS) AND PROXIMAL TO D17S856 ON CHROMOSOME 17Q12-Q21
Genomics
MULTIPOINT RADIATION HYBRID MAPPING - COMPARISON OF METHODS, SAMPLE-SIZE REQUIREMENTS, AND OPTIMAL STUDY CHARACTERISTICS
Genomics
LINKAGE ANALYSIS OF MAJOR HISTOCOMPATIBILITY GENES IN FAMILIAL SARCOIDOSIS
Sarcoidosis
MAPPING WITH MICROSATELLITE REPEAT MARKERS ON PROXIMAL 1Q
Cytogenetics and cell genetics
IN-VITRO TOXICITY OF POLYHEXANIDE (PHMB)
Investigative ophthalmology & visual science
FAMILIAL GLAUCOMA - THE STOKES PEDIGREE REVISITED
Investigative ophthalmology & visual science
LINKAGE ANALYSIS OF AUTOSOMAL-DOMINANT JUVENILE-ONSET OPEN-ANGLE GLAUCOMA IN AN OHIO FAMILY
Investigative ophthalmology & visual science
MEASUREMENT OF ENDOTHELIAL BARRIER FUNCTION BY TRANSENDOTHELIAL ACCUMULATION OF STROMAL FLUORESCEIN
Investigative ophthalmology & visual science
RISKS OF CANCER IN BRCA1-MUTATION CARRIERS
Lancet
2-LOCUS VERSUS ONE-LOCUS LODS FOR COMPLEX TRAITS - REPLY
American journal of human genetics
LIMITS OF RESOLUTION OF GENETIC-LINKAGE STUDIES - IMPLICATIONS FOR THE POSITIONAL CLONING OF HUMAN-DISEASE GENES
American journal of human genetics
THE APOLIPOPROTEIN E CI/CII GENE-CLUSTER AND LATE-ONSET ALZHEIMER-DISEASE/
American journal of human genetics
MAPPING OF A GENE FOR AUTOSOMAL-DOMINANT JUVENILE-ONSET OPEN-ANGLE GLAUCOMA TO CHROMOSOME-IQ
American journal of human genetics
MULTICOLOR FISH MAPPING WITH ALU-PCR-AMPLIFIED YAC CLONE DNA DETERMINES THE ORDER OF MARKERS IN THE BRCA1 REGION ON CHROMOSOME-17Q12-Q21
Genomics
A RADIATION HYBRID MAP OF THE BRCA1 REGION OF CHROMOSOME-17Q12-Q21
Genomics
GENETIC-COUNSELING FOR FAMILIES WITH INHERITED SUSCEPTIBILITY TO BREAST AND OVARIAN-CANCER (VOL 269, PG 1970, 1993)
JAMA, the journal of the American Medical Association
2-TRAIT-LOCUS LINKAGE ANALYSIS - A POWERFUL STRATEGY FOR MAPPING COMPLEX GENETIC-TRAITS
American journal of human genetics
FAMILIAL ALZHEIMERS-DISEASE AND GENETIC-HETEROGENEITY
American journal of human genetics
GENETIC-LINKAGE OF HEREDITARY HEMORRHAGIC TELANGIECTASIA TO MARKERS ON 9Q
American journal of human genetics
LIMITS OF RESOLUTION OF HUMAN LINKAGE STUDIES - IMPLICATIONS FOR THE POSITIONAL CLONING OF DISEASE GENES
American journal of human genetics
THE POSTERIOR PROBABILITY OF LINKAGE
American journal of human genetics
GENETIC-LINKAGE AROUND X-LINKED RETINOSCHISIS (RS)
American journal of human genetics
RELATIVE EFFICIENCY AND POWER OF LOD SCORE AND SIB-PAIR METHODS OF LINKAGE ANALYSIS
American journal of human genetics
BEST MACULAR DEGENERATION (BMD) - LINKAGE AND ROM1 CANDIDATE GENE SEQUENCING
American journal of human genetics