VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q64183498 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241121000234.0
008 241121nneanz||abbn n and d
035 ‎‡a (WKP)Q64183498‏
024 ‎‡a 0000-0002-8819-2443‏ ‎‡2 orcid‏
035 ‎‡a (OCoLC)Q64183498‏
100 0 ‎‡a Chun Li‏ ‎‡c researcher ORCID 0000-0002-8819-2443‏ ‎‡9 en‏
400 0 ‎‡a Chun Li‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
670 ‎‡a Author's A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14‏
670 ‎‡a Author's A new residual for ordinal outcomes‏
670 ‎‡a Author's A novel, noninvasive assay shows that distal airway oxygen tension is low in cystic fibrosis, but not in primary ciliary dyskinesia‏
670 ‎‡a Author's A powerful association test of multiple genetic variants using a random-effects model.‏
670 ‎‡a Author's A prevalence-based association test for case-control studies.‏
670 ‎‡a Author's A statistical reappraisal of the findings of an esophageal cancer genome-wide association study‏
670 ‎‡a Author's A variant in the osteoprotegerin gene is associated with coronary atherosclerosis in patients with rheumatoid arthritis: results from a candidate gene study‏
670 ‎‡a Author's Alpha2A adrenergic receptor genetic variation contributes to hyperglycemia after myocardial infarction‏
670 ‎‡a Author's Association of genetic variation with blood pressure traits among East Africans.‏
670 ‎‡a Author's Associations of plasma-soluble fas ligand with aging and age-related macular degeneration‏
670 ‎‡a Author's Beta-1-adrenoceptor genetic variants and ethnicity independently affect response to beta-blockade.‏
670 ‎‡a Author's Catecholamine pathway gene variation is associated with norepinephrine and epinephrine concentrations at rest and after exercise.‏
670 ‎‡a Author's Covariate-adjusted Spearman's rank correlation with probability-scale residuals.‏
670 ‎‡a Author's Design of DNA pooling to allow incorporation of covariates in rare variants analysis‏
670 ‎‡a Author's Detecting gene-gene interaction in linkage analysis.‏
670 ‎‡a Author's Effect of the VKORC1 D36Y variant on warfarin dose requirement and pharmacogenetic dose prediction.‏
670 ‎‡a Author's Effects of environment, genetics and data analysis pitfalls in an esophageal cancer genome-wide association study.‏
670 ‎‡a Author's Efficacy of Abiraterone and Enzalutamide in Pre- and Postdocetaxel Castration-Resistant Prostate Cancer: A Trial-Level Meta-Analysis.‏
670 ‎‡a Author's Enriching targeted sequencing experiments for rare disease alleles.‏
670 ‎‡a Author's Estrogen exposure, metabolism, and enzyme variants in a model for breast cancer risk prediction.‏
670 ‎‡a Author's First-time failure rates of candidates for board certification: an educational outcome measure‏
670 ‎‡a Author's Genetic association analysis using data from triads and unrelated subjects‏
670 ‎‡a Author's Genetic polymorphisms in the IGFBP3 gene: association with breast cancer risk and blood IGFBP-3 protein levels among Chinese women.‏
670 ‎‡a Author's Genetic variation and coronary atherosclerosis in patients with systemic lupus erythematosus‏
670 ‎‡a Author's Genetic variation in the Alpha 1B-adrenergic receptor and vascular response.‏
670 ‎‡a Author's Genetic variation in the presynaptic norepinephrine transporter is associated with blood pressure responses to exercise in healthy humans‏
670 ‎‡a Author's Genetic variation in the α1A-adrenergic receptor and phenylephrine-mediated venoconstriction.‏
670 ‎‡a Author's Genetic variation near the hepatocyte nuclear factor-4 Alpha gene predicts susceptibility to type 2 diabetes‏
670 ‎‡a Author's Genetic variations in the α‏
670 ‎‡a Author's Genetic variations in the α(2A)-adrenoreceptor are associated with blood pressure response to the agonist dexmedetomidine‏
670 ‎‡a Author's Genetics of serum concentration of IL-6 and TNFα in systemic lupus erythematosus and rheumatoid arthritis: a candidate gene analysis‏
670 ‎‡a Author's Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202‏
670 ‎‡a Author's Genotype and risk of major bleeding during warfarin treatment‏
670 ‎‡a Author's GRK5 Gln41Leu polymorphism is not associated with sensitivity to beta(1)-adrenergic blockade in humans.‏
670 ‎‡a Author's Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization‏
670 ‎‡a Author's Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium‏
670 ‎‡a Author's Identification of new genetic risk variants for type 2 diabetes‏
670 ‎‡a Author's Joint analyses of multi-tissue Hi-C and eQTL data demonstrate close spatial proximity between eQTLs and their target genes‏
670 ‎‡a Author's Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk‏
670 ‎‡a Author's Longitudinal follow-up of hypermetropic children identified during preschool vision screening.‏
670 ‎‡a Author's Meta-analysis identifies common variants associated with body mass index in east Asians‏
670 ‎‡a Author's Modeling continuous response variables using ordinal regression‏
670 ‎‡a Author's Morphometric changes in the rat optic nerve following short-term intermittent elevations in intraocular pressure.‏
670 ‎‡a Author's Optimized selection of unrelated subjects for whole-genome sequencing studies of rare high-penetrance alleles.‏
670 ‎‡a Author's Probability-scale residuals for continuous, discrete, and censored data‏
670 ‎‡a Author's Racial disparity in amniotic fluid concentrations of tumor necrosis factor‏
670 ‎‡a Author's Racial disparity in amniotic fluid concentrations of tumor necrosis factor (TNF)- Alpha and soluble TNF receptors in spontaneous preterm birth.‏
670 ‎‡a Author's Soft Tissue Metrics in Thyroid Eye Disease: An International Thyroid Eye Disease Society Reliability Study.‏
670 ‎‡a Author's Strategy for encoding and comparison of gene expression signatures.‏
670 ‎‡a Author's Test of Association Between Two Ordinal Variables While Adjusting for Covariates‏
670 ‎‡a Author's Tgif1 regulates quiescence and self-renewal of hematopoietic stem cells‏
670 ‎‡a Author's The age-dependent effect of anisometropia magnitude on anisometropic amblyopia severity‏
670 ‎‡a Author's The failure rate of candidates for board certification: an educational outcome measure.‏
670 ‎‡a Author's The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics‏
670 ‎‡a Author's 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.‏
670 ‎‡a Author's Underestimation of soft tissue entrapment by computed tomography in orbital floor fractures in the pediatric population.‏
670 ‎‡a Author's Use of cox-2 inhibitors in patients with retinal venous occlusive disease.‏
670 ‎‡a Author's Variations in the Alpha 2A-adrenergic receptor gene and their functional effects.‏
909 ‎‡a (orcid) 0000000288192443‏ ‎‡9 1‏
912 ‎‡a heightandbreastcancerriskevidencefromprospectivestudiesandmendelianrandomization‏ ‎‡A Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization‏ ‎‡9 1‏
919 ‎‡a strategyforencodingandcomparisonofgeneexpressionsignatures‏ ‎‡A Strategy for encoding and comparison of gene expression signatures.‏ ‎‡9 1‏
919 ‎‡a testofassociationbetween2ordinalvariableswhileadjustingforcovariates‏ ‎‡A Test of Association Between Two Ordinal Variables While Adjusting for Covariates‏ ‎‡9 1‏
919 ‎‡a tgif1regulatesquiescenceandselfrenewalofhematopoieticstemcells‏ ‎‡A Tgif1 regulates quiescence and self-renewal of hematopoietic stem cells‏ ‎‡9 1‏
919 ‎‡a agedependenteffectofanisometropiamagnitudeonanisometropicamblyopiaseverity‏ ‎‡A The age-dependent effect of anisometropia magnitude on anisometropic amblyopia severity‏ ‎‡9 1‏
919 ‎‡a failurerateofcandidatesforboardcertificationaneducationaloutcomemeasure‏ ‎‡A The failure rate of candidates for board certification: an educational outcome measure.‏ ‎‡9 1‏
919 ‎‡a variationsinthe Alpha 2aadrenergicreceptorgeneandtheirfunctionaleffects‏ ‎‡A Variations in the Alpha 2A-adrenergic receptor gene and their functional effects.‏ ‎‡9 1‏
919 ‎‡a finlandunitedstatesinvestigationofnoninsulindependentdiabetesmellitusgenetics‏ ‎‡A The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics‏ ‎‡9 1‏
919 ‎‡a effectofthevkorc1d36yvariantonwarfarindoserequirementandpharmacogeneticdoseprediction‏ ‎‡A Effect of the VKORC1 D36Y variant on warfarin dose requirement and pharmacogenetic dose prediction.‏ ‎‡9 1‏
919 ‎‡a efficacyofabirateroneandenzalutamideinpreandpostdocetaxelcastrationresistantprostatecanceratriallevelmetaanalysis‏ ‎‡A Efficacy of Abiraterone and Enzalutamide in Pre- and Postdocetaxel Castration-Resistant Prostate Cancer: A Trial-Level Meta-Analysis.‏ ‎‡9 1‏
919 ‎‡a enrichingtargetedsequencingexperimentsforrarediseasealleles‏ ‎‡A Enriching targeted sequencing experiments for rare disease alleles.‏ ‎‡9 1‏
919 ‎‡a estrogenexposuremetabolismandenzymevariantsinamodelforbreastcancerriskprediction‏ ‎‡A Estrogen exposure, metabolism, and enzyme variants in a model for breast cancer risk prediction.‏ ‎‡9 1‏
919 ‎‡a 1timefailureratesofcandidatesforboardcertificationaneducationaloutcomemeasure‏ ‎‡A First-time failure rates of candidates for board certification: an educational outcome measure‏ ‎‡9 1‏
919 ‎‡a newresidualforordinaloutcomes‏ ‎‡A A new residual for ordinal outcomes‏ ‎‡9 1‏
919 ‎‡a novelnoninvasiveassayshowsthatdistalairwayoxygentensionislowincysticfibrosisbutnotinprimaryciliarydyskinesia‏ ‎‡A A novel, noninvasive assay shows that distal airway oxygen tension is low in cystic fibrosis, but not in primary ciliary dyskinesia‏ ‎‡9 1‏
919 ‎‡a finlandunitedstatesinvestigationofnoninsulindependentdiabetesmellitusgeneticsfusionstudy2anautosomalgenomescanfordiabetesrelatedquantitativetraitloci‏ ‎‡A 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.‏ ‎‡9 1‏
919 ‎‡a underestimationofsofttissueentrapmentbycomputedtomographyinorbitalfloorfracturesinthepediatricpopulation‏ ‎‡A Underestimation of soft tissue entrapment by computed tomography in orbital floor fractures in the pediatric population.‏ ‎‡9 1‏
919 ‎‡a useofcox2inhibitorsinpatientswithretinalvenousocclusivedisease‏ ‎‡A Use of cox-2 inhibitors in patients with retinal venous occlusive disease.‏ ‎‡9 1‏
919 ‎‡a geneticassociationanalysisusingdatafromtriadsandunrelatedsubjects‏ ‎‡A Genetic association analysis using data from triads and unrelated subjects‏ ‎‡9 1‏
919 ‎‡a geneticpolymorphismsintheigfbp3geneassociationwithbreastcancerriskandbloodigfbp3proteinlevelsamongchinesewomen‏ ‎‡A Genetic polymorphisms in the IGFBP3 gene: association with breast cancer risk and blood IGFBP-3 protein levels among Chinese women.‏ ‎‡9 1‏
919 ‎‡a geneticvariationandcoronaryatherosclerosisinpatientswithsystemiclupuserythematosus‏ ‎‡A Genetic variation and coronary atherosclerosis in patients with systemic lupus erythematosus‏ ‎‡9 1‏
919 ‎‡a powerfulassociationtestofmultiplegeneticvariantsusingarandomeffectsmodel‏ ‎‡A A powerful association test of multiple genetic variants using a random-effects model.‏ ‎‡9 1‏
919 ‎‡a geneticvariationinthe Alpha 1badrenergicreceptorandvascularresponse‏ ‎‡A Genetic variation in the Alpha 1B-adrenergic receptor and vascular response.‏ ‎‡9 1‏
919 ‎‡a geneticvariationinthepresynapticnorepinephrinetransporterisassociatedwithbloodpressureresponsestoexerciseinhealthyhumans‏ ‎‡A Genetic variation in the presynaptic norepinephrine transporter is associated with blood pressure responses to exercise in healthy humans‏ ‎‡9 1‏
919 ‎‡a prevalencebasedassociationtestforcasecontrolstudies‏ ‎‡A A prevalence-based association test for case-control studies.‏ ‎‡9 1‏
919 ‎‡a geneticvariationintheα1aadrenergicreceptorandphenylephrinemediatedvenoconstriction‏ ‎‡A Genetic variation in the α1A-adrenergic receptor and phenylephrine-mediated venoconstriction.‏ ‎‡9 1‏
919 ‎‡a statisticalreappraisalofthefindingsofanesophagealcancergenomewideassociationstudy‏ ‎‡A A statistical reappraisal of the findings of an esophageal cancer genome-wide association study‏ ‎‡9 1‏
919 ‎‡a geneticvariationnearthehepatocytenuclearfactor4 Alpha genepredictssusceptibilitytotype2diabetes‏ ‎‡A Genetic variation near the hepatocyte nuclear factor-4 Alpha gene predicts susceptibility to type 2 diabetes‏ ‎‡9 1‏
919 ‎‡a geneticvariationsintheα‏ ‎‡A Genetic variations in the α‏ ‎‡9 1‏
919 ‎‡a geneticvariationsintheα2aadrenoreceptorareassociatedwithbloodpressureresponsetotheagonistdexmedetomidine‏ ‎‡A Genetic variations in the α(2A)-adrenoreceptor are associated with blood pressure response to the agonist dexmedetomidine‏ ‎‡9 1‏
919 ‎‡a geneticsofserumconcentrationofil6andtnfαinsystemiclupuserythematosusandrheumatoidarthritisacandidategeneanalysis‏ ‎‡A Genetics of serum concentration of IL-6 and TNFα in systemic lupus erythematosus and rheumatoid arthritis: a candidate gene analysis‏ ‎‡9 1‏
919 ‎‡a genomewideassociationstudyoftenofovirpharmacokineticsandcreatinineclearanceinaidsclinicaltrialsgroupprotocol‏ ‎‡A Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202‏ ‎‡9 1‏
919 ‎‡a genotypeandriskofmajorbleedingduringwarfarintreatment‏ ‎‡A Genotype and risk of major bleeding during warfarin treatment‏ ‎‡9 1‏
919 ‎‡a grk5gln41leupolymorphismisnotassociatedwithsensitivitytobeta1adrenergicblockadeinhumans‏ ‎‡A GRK5 Gln41Leu polymorphism is not associated with sensitivity to beta(1)-adrenergic blockade in humans.‏ ‎‡9 1‏
919 ‎‡a identificationofafunctionalgeneticvariantat16q121forbreastcancerriskresultsfromtheasiabreastcancerconsortium‏ ‎‡A Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium‏ ‎‡9 1‏
919 ‎‡a identificationofnewgeneticriskvariantsfortype2diabetes‏ ‎‡A Identification of new genetic risk variants for type 2 diabetes‏ ‎‡9 1‏
919 ‎‡a jointanalysesofmultitissuehi100andeqtldatademonstrateclosespatialproximitybetweeneqtlsandtheirtargetgenes‏ ‎‡A Joint analyses of multi-tissue Hi-C and eQTL data demonstrate close spatial proximity between eQTLs and their target genes‏ ‎‡9 1‏
919 ‎‡a largescalegeneticstudyineastasiansidentifies6newlociassociatedwithcolorectalcancerrisk‏ ‎‡A Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk‏ ‎‡9 1‏
919 ‎‡a longitudinalfollowupofhypermetropicchildrenidentifiedduringpreschoolvisionscreening‏ ‎‡A Longitudinal follow-up of hypermetropic children identified during preschool vision screening.‏ ‎‡9 1‏
919 ‎‡a metaanalysisidentifiescommonvariantsassociatedwithbodymassindexineastasians‏ ‎‡A Meta-analysis identifies common variants associated with body mass index in east Asians‏ ‎‡9 1‏
919 ‎‡a modelingcontinuousresponsevariablesusingordinalregression‏ ‎‡A Modeling continuous response variables using ordinal regression‏ ‎‡9 1‏
919 ‎‡a morphometricchangesintheratopticnervefollowingshorttermintermittentelevationsinintraocularpressure‏ ‎‡A Morphometric changes in the rat optic nerve following short-term intermittent elevations in intraocular pressure.‏ ‎‡9 1‏
919 ‎‡a optimizedselectionofunrelatedsubjectsforwholegenomesequencingstudiesofrarehighpenetrancealleles‏ ‎‡A Optimized selection of unrelated subjects for whole-genome sequencing studies of rare high-penetrance alleles.‏ ‎‡9 1‏
919 ‎‡a probabilityscaleresidualsforcontinuousdiscreteandcensoreddata‏ ‎‡A Probability-scale residuals for continuous, discrete, and censored data‏ ‎‡9 1‏
919 ‎‡a racialdisparityinamnioticfluidconcentrationsoftumornecrosisfactor‏ ‎‡A Racial disparity in amniotic fluid concentrations of tumor necrosis factor‏ ‎‡9 1‏
919 ‎‡a racialdisparityinamnioticfluidconcentrationsoftumornecrosisfactortnf Alpha andsolubletnfreceptorsinspontaneouspretermbirth‏ ‎‡A Racial disparity in amniotic fluid concentrations of tumor necrosis factor (TNF)- Alpha and soluble TNF receptors in spontaneous preterm birth.‏ ‎‡9 1‏
919 ‎‡a variantintheosteoprotegeringeneisassociatedwithcoronaryatherosclerosisinpatientswithrheumatoidarthritisresultsfromacandidategenestudy‏ ‎‡A A variant in the osteoprotegerin gene is associated with coronary atherosclerosis in patients with rheumatoid arthritis: results from a candidate gene study‏ ‎‡9 1‏
919 ‎‡a Alpha 2aadrenergicreceptorgeneticvariationcontributestohyperglycemiaaftermyocardialinfarction‏ ‎‡A Alpha2A adrenergic receptor genetic variation contributes to hyperglycemia after myocardial infarction‏ ‎‡9 1‏
919 ‎‡a associationofgeneticvariationwithbloodpressuretraitsamongeastafricans‏ ‎‡A Association of genetic variation with blood pressure traits among East Africans.‏ ‎‡9 1‏
919 ‎‡a associationsofplasmasolublefasligandwithagingandagerelatedmaculardegeneration‏ ‎‡A Associations of plasma-soluble fas ligand with aging and age-related macular degeneration‏ ‎‡9 1‏
919 ‎‡a beta1adrenoceptorgeneticvariantsandethnicityindependentlyaffectresponsetobetablockade‏ ‎‡A Beta-1-adrenoceptor genetic variants and ethnicity independently affect response to beta-blockade.‏ ‎‡9 1‏
919 ‎‡a catecholaminepathwaygenevariationisassociatedwithnorepinephrineandepinephrineconcentrationsatrestandafterexercise‏ ‎‡A Catecholamine pathway gene variation is associated with norepinephrine and epinephrine concentrations at rest and after exercise.‏ ‎‡9 1‏
919 ‎‡a largesetoffinnishaffectedsiblingpairfamilieswithtype2diabetessuggestssusceptibilitylocionchromosomes611and14‏ ‎‡A A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14‏ ‎‡9 1‏
919 ‎‡a covariateadjustedspearmansrankcorrelationwithprobabilityscaleresiduals‏ ‎‡A Covariate-adjusted Spearman's rank correlation with probability-scale residuals.‏ ‎‡9 1‏
919 ‎‡a designofdnapoolingtoallowincorporationofcovariatesinrarevariantsanalysis‏ ‎‡A Design of DNA pooling to allow incorporation of covariates in rare variants analysis‏ ‎‡9 1‏
919 ‎‡a detectinggenegeneinteractioninlinkageanalysis‏ ‎‡A Detecting gene-gene interaction in linkage analysis.‏ ‎‡9 1‏
919 ‎‡a softtissuemetricsinthyroideyediseaseaninternationalthyroideyediseasesocietyreliabilitystudy‏ ‎‡A Soft Tissue Metrics in Thyroid Eye Disease: An International Thyroid Eye Disease Society Reliability Study.‏ ‎‡9 1‏
919 ‎‡a effectsofenvironmentgeneticsanddataanalysispitfallsinanesophagealcancergenomewideassociationstudy‏ ‎‡A Effects of environment, genetics and data analysis pitfalls in an esophageal cancer genome-wide association study.‏ ‎‡9 1‏
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996 ‎‡2 ISNI|0000000045770317‏
996 ‎‡2 LC|nr 97005366‏
996 ‎‡2 NII|DA11659771‏
996 ‎‡2 SUDOC|234769742‏
996 ‎‡2 ISNI|0000000037737349‏
996 ‎‡2 ISNI|0000000367196362‏
996 ‎‡2 DNB|1016394632‏
996 ‎‡2 CYT|AC000216875‏
996 ‎‡2 DNB|1315156172‏
996 ‎‡2 CYT|AC000418158‏
996 ‎‡2 DNB|1227483570‏
996 ‎‡2 LC|n 2018007848‏
996 ‎‡2 DNB|135702828‏
996 ‎‡2 CYT|AC000632559‏
996 ‎‡2 BNF|17014662‏
996 ‎‡2 ISNI|0000000063614756‏
996 ‎‡2 CYT|AC000495556‏
996 ‎‡2 LNB|LNC10-000258680‏
996 ‎‡2 SUDOC|03396145X‏
996 ‎‡2 SUDOC|122151372‏
996 ‎‡2 ISNI|0000000064248436‏
996 ‎‡2 BNF|15108025‏
996 ‎‡2 BIBSYS|1632996806229‏
996 ‎‡2 LC|n 2016023097‏
996 ‎‡2 DNB|131063937X‏
996 ‎‡2 BIBSYS|90738495‏
996 ‎‡2 LC|no2019068892‏
996 ‎‡2 ISNI|0000000381698094‏
996 ‎‡2 NUKAT|n 2012240690‏
996 ‎‡2 CYT|AC000475627‏
996 ‎‡2 ISNI|0000000083312501‏
996 ‎‡2 LC|no2008107022‏
996 ‎‡2 LC|no2004062396‏
996 ‎‡2 NTA|323265480‏
996 ‎‡2 LC|n 88194944‏
996 ‎‡2 NII|DA07806329‏
996 ‎‡2 ISNI|0000000063269710‏
996 ‎‡2 CYT|AC000591572‏
996 ‎‡2 LC|nr 96028617‏
996 ‎‡2 CYT|AC000552631‏
996 ‎‡2 SUDOC|116005297‏
996 ‎‡2 DNB|128264064X‏
996 ‎‡2 LC|n 90643389‏
996 ‎‡2 ISNI|0000000064219088‏
996 ‎‡2 LC|n 2005063562‏
996 ‎‡2 NTA|207215286‏
996 ‎‡2 NTA|364154128‏
996 ‎‡2 DNB|1089651414‏
996 ‎‡2 ISNI|0000000063778363‏
996 ‎‡2 CYT|AC000590194‏
996 ‎‡2 SUDOC|231560982‏
996 ‎‡2 CYT|AC000643250‏
996 ‎‡2 NII|DA10337816‏
996 ‎‡2 ISNI|0000000458776549‏
996 ‎‡2 ISNI|0000000076750642‏
996 ‎‡2 J9U|987007345960405171‏
996 ‎‡2 DNB|1171334788‏
996 ‎‡2 LC|no 97059411‏
996 ‎‡2 SUDOC|117561886‏
996 ‎‡2 ISNI|0000000043567809‏
996 ‎‡2 ISNI|0000000051709221‏
996 ‎‡2 PLWABN|9814258275005606‏
996 ‎‡2 DNB|1157497802‏
996 ‎‡2 NTA|382731549‏
996 ‎‡2 LC|no2018144101‏
996 ‎‡2 PLWABN|9813224594305606‏
996 ‎‡2 ISNI|0000000074185846‏
996 ‎‡2 NUKAT|n 2015183984‏
996 ‎‡2 LC|n 78041880‏
996 ‎‡2 CYT|AC000454499‏
996 ‎‡2 LNB|LNC10-000202245‏
996 ‎‡2 DNB|102379425X‏
996 ‎‡2 J9U|987007431582205171‏
996 ‎‡2 LC|n 2003002518‏
996 ‎‡2 ISNI|0000000052187656‏
996 ‎‡2 ISNI|0000000107997163‏
996 ‎‡2 PLWABN|9810560077905606‏
996 ‎‡2 SUDOC|193884305‏
996 ‎‡2 ISNI|0000000381957383‏
996 ‎‡2 LC|n 84132772‏
996 ‎‡2 KRNLK|KAC200709106‏
996 ‎‡2 LC|no2006036555‏
996 ‎‡2 ISNI|000000006427751X‏
996 ‎‡2 LC|no 98066212‏
996 ‎‡2 CYT|AC000660749‏
996 ‎‡2 BNF|15045297‏
996 ‎‡2 ISNI|0000000063447580‏
996 ‎‡2 LC|n 2007047655‏
996 ‎‡2 PLWABN|9812807240505606‏
996 ‎‡2 LC|nr 96020721‏
996 ‎‡2 LC|no2023068189‏
996 ‎‡2 LC|nr 88001082‏
996 ‎‡2 SUDOC|157288552‏
997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏