VIAF

Virtual International Authority File

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Leader     00000nz a2200037n 45 0
001     WKP|Q56747987  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241221010844.0
008     241221nneanz||abbn n and d
035 ‎‡a  (WKP)Q56747987‏
024 ‎‡a  0000-0001-9546-4614‏ ‎‡2  orcid‏
024 ‎‡a  7103069682‏ ‎‡2  scopus‏
035 ‎‡a  (OCoLC)Q56747987‏
100 0 ‎‡a  Filipa Carvalho‏ ‎‡c  researcher (ORCID 0000-0001-9546-4614)‏ ‎‡9  en‏
400 0 ‎‡a  Filipa Carvalho‏ ‎‡c  onderzoeker‏ ‎‡9  nl‏
670 ‎‡a  Author's A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia‏
670 ‎‡a  Author's A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens‏
670 ‎‡a  Author's Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia‏
670 ‎‡a  Author's An efficient protocol for the detection of chromosomal abnormalities in spontaneous miscarriages or foetal deaths‏
670 ‎‡a  Author's Aneuploidies Detection in Miscarriages and Fetal Deaths Using Multiplex Ligation-Dependent Probe Amplification: An Alternative for Speeding up Results?‏
670 ‎‡a  Author's Application of touch FISH in the study of mosaic tetraploidy and maternal cell contamination in pregnancy losses‏
670 ‎‡a  Author's Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens‏
670 ‎‡a  Author's AZF and DAZ gene copy-specific deletion analysis in maturation arrest and Sertoli cell-only syndrome‏
670 ‎‡a  Author's Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia‏
670 ‎‡a  Author's Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly‏
670 ‎‡a  Author's Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens‏
670 ‎‡a  Author's Characterization of missense mutations and large deletions in the ALPL gene by sequencing and quantitative multiplex PCR of short fragments.‏
670 ‎‡a  Author's Clinical outcomes after preimplantation genetic diagnosis of patients with Corino de Andrade disease‏
670 ‎‡a  Author's Clinical outcomes after preimplantation genetic diagnosis of patients with Corino de Andrade disease (familial amyloid polyneuropathy).‏
670 ‎‡a  Author's Cytological and expression studies and quantitative analysis of the temporal and stage-specific effects of follicle-stimulating hormone and testosterone during cocultures of the normal human seminiferous epithelium.‏
670 ‎‡a  Author's DNA methylation imprinting errors in spermatogenic cells from maturation arrest azoospermic patients‏
670 ‎‡a  Author's DNA methylation imprinting marks and DNA methyltransferase expression in human spermatogenic cell stages‏
670 ‎‡a  Author's Early Gestational Diagnosis of Lethal Skeletal Dysplasias: A 15 Year Retrospective Cohort Reviewing Concordance between Ultrasonographic, Genetic and Morphological Features‏
670 ‎‡a  Author's Effect of single-nucleotide polymorphisms of the 5' untranslated region of the human α-galactosidase gene on enzyme activity, and their frequencies in Portuguese caucasians.‏
670 ‎‡a  Author's ESHRE PGT Consortium data collection XIX-XX: PGT analyses from 2016 to 2017<sup>†</sup>‏
670 ‎‡a  Author's ESHRE PGT Consortium good practice recommendations for the detection of monogenic disorders‏
670 ‎‡a  Author's Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study.‏
670 ‎‡a  Author's Expression of stem cell markers: OCT4, KIT, ITGA6, and ITGB1 in the male germinal epithelium.‏
670 ‎‡a  Author's Genetic regulation on ex vivo differentiated natural killer cells from human umbilical cord blood CD34+ cells‏
670 ‎‡a  Author's Genomic imprinting in disruptive spermatogenesis‏
670 ‎‡a  Author's Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.‏
670 ‎‡a  Author's Immunohistochemical study of the expression of MUC6 mucin and co-expression of other secreted mucins‏
670 ‎‡a  Author's Immunohistochemical study of the expression of MUC6 mucin and co-expression of other secreted mucins (MUC5AC and MUC2) in human gastric carcinomas‏
670 ‎‡a  Author's Keratitis-Ichthyosis-Deafness Syndrome Caused by GJB2 Maternal Mosaicism‏
670 ‎‡a  Author's Methylation defects of imprinted genes in human testicular spermatozoa‏
670 ‎‡a  Author's Molecular and functional characterization of CBAVD-causing mutations located in CFTR nucleotide-binding domains‏
670 ‎‡a  Author's Molecular characterization of the cystic fibrosis transmembrane conductance regulator gene in congenital absence of the vas deferens‏
670 ‎‡a  Author's MUC1 gene polymorphism and gastric cancer--an epidemiological study.‏
670 ‎‡a  Author's MUC1 gene polymorphism in the gastric carcinogenesis pathway.‏
670 ‎‡a  Author's MUC1 polymorphism confers increased risk for intestinal metaplasia in a Colombian population with chronic gastritis‏
670 ‎‡a  Author's MUC6 gene polymorphism in healthy individuals and in gastric cancer patients from northern Portugal.‏
670 ‎‡a  Author's Mucins and mucin-associated carbohydrate antigens expression in gastric carcinoma cell lines‏
670 ‎‡a  Author's Novel human pathological mutations. Gene symbol: GLA. Disease: Fabry disease‏
670 ‎‡a  Author's Phenotypic expression in the first case of complete trisomy 12: combination of prenatal ultrasound and necropsic examination‏
670 ‎‡a  Author's Quantitative analysis of cellular proliferation and differentiation of the human seminiferous epithelium in vitro‏
670 ‎‡a  Author's Rare double sex and mab-3-related transcription factor 1 regulatory variants in severe spermatogenic failure‏
670 ‎‡a  Author's Relevance of genomic imprinting in intrauterine human growth expression of CDKN1C, H19, IGF2, KCNQ1 and PHLDA2 imprinted genes‏
670 ‎‡a  Author's Semen quality is affected by HLA class I alleles together with sexually transmitted diseases‏
670 ‎‡a  Author's Sequence diversity at the proximal 14q32.1 SERPIN subcluster: evidence for natural selection favoring the pseudogenization of SERPINA2.‏
670 ‎‡a  Author's Sequence variation at KLK and WFDC clusters and its association to semen hyperviscosity and other male infertility phenotypes‏
670 ‎‡a  Author's Spectrum of CFTR gene sequence variants in a northern Portugal population‏
670 ‎‡a  Author's The clinical utility of PGD with HLA matching: a collaborative multi-centre ESHRE study‏
670 ‎‡a  Author's The g.1170C>T polymorphism of the 5' untranslated region of the human alpha-galactosidase gene is associated with decreased enzyme expression--evidence from a family study‏
670 ‎‡a  Author's The mutational spectrum of WT1 in male infertility.‏
670 ‎‡a  Author's Treatment by testicular sperm extraction and intracytoplasmic sperm injection of 65 azoospermic patients with non-mosaic Klinefelter syndrome with birth of 17 healthy children‏
670 ‎‡a  Author's Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies‏
909 ‎‡a  (scopus) 7103069682‏ ‎‡9  1‏
909 ‎‡a  (orcid) 0000000195464614‏ ‎‡9  1‏
919 ‎‡a  novelalumediatedmicrodeletionat11p13removeswt1inapatientwithcryptorchidismandazoospermia‏ ‎‡A  A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia‏ ‎‡9  1‏
919 ‎‡a  cytologicalandexpressionstudiesandquantitativeanalysisofthetemporalandstagespecificeffectsoffolliclestimulatinghormoneandtestosteroneduringcoculturesofthenormalhumanseminiferousepithelium‏ ‎‡A  Cytological and expression studies and quantitative analysis of the temporal and stage-specific effects of follicle-stimulating hormone and testosterone during cocultures of the normal human seminiferous epithelium.‏ ‎‡9  1‏
919 ‎‡a  dnamethylationimprintingerrorsinspermatogeniccellsfrommaturationarrestazoospermicpatients‏ ‎‡A  DNA methylation imprinting errors in spermatogenic cells from maturation arrest azoospermic patients‏ ‎‡9  1‏
919 ‎‡a  clinicaloutcomesafterpreimplantationgeneticdiagnosisofpatientswithcorinodeandradediseasefamilialamyloidpolyneuropathy‏ ‎‡A  Clinical outcomes after preimplantation genetic diagnosis of patients with Corino de Andrade disease (familial amyloid polyneuropathy).‏ ‎‡9  1‏
919 ‎‡a  dnamethylationimprintingmarksanddnamethyltransferaseexpressioninhumanspermatogeniccellstages‏ ‎‡A  DNA methylation imprinting marks and DNA methyltransferase expression in human spermatogenic cell stages‏ ‎‡9  1‏
919 ‎‡a  novelmissensemutationp1290satexon20ofthecftrgeneinaportuguesepatientwithcongenitalbilateralabsenceofthevasdeferens‏ ‎‡A  A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens‏ ‎‡9  1‏
919 ‎‡a  earlygestationaldiagnosisoflethalskeletaldysplasiasa15yearretrospectivecohortreviewingconcordancebetweenultrasonographicgeneticandmorphologicalfeatures‏ ‎‡A  Early Gestational Diagnosis of Lethal Skeletal Dysplasias: A 15 Year Retrospective Cohort Reviewing Concordance between Ultrasonographic, Genetic and Morphological Features‏ ‎‡9  1‏
919 ‎‡a  clinicaloutcomesafterpreimplantationgeneticdiagnosisofpatientswithcorinodeandradedisease‏ ‎‡A  Clinical outcomes after preimplantation genetic diagnosis of patients with Corino de Andrade disease‏ ‎‡9  1‏
919 ‎‡a  abnormalmethylationofimprintedgenesinhumanspermisassociatedwitholigozoospermia‏ ‎‡A  Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia‏ ‎‡9  1‏
919 ‎‡a  effectofsinglenucleotidepolymorphismsofthe5untranslatedregionofthehumanαgalactosidasegeneonenzymeactivityandtheirfrequenciesinportuguesecaucasians‏ ‎‡A  Effect of single-nucleotide polymorphisms of the 5' untranslated region of the human α-galactosidase gene on enzyme activity, and their frequencies in Portuguese caucasians.‏ ‎‡9  1‏
919 ‎‡a  efficientprotocolforthedetectionofchromosomalabnormalitiesinspontaneousmiscarriagesorfoetaldeaths‏ ‎‡A  An efficient protocol for the detection of chromosomal abnormalities in spontaneous miscarriages or foetal deaths‏ ‎‡9  1‏
919 ‎‡a  eshrepgtconsortiumdatacollection1920pgtanalysesfrom2016to2017supsup‏ ‎‡A  ESHRE PGT Consortium data collection XIX-XX: PGT analyses from 2016 to 2017<sup>†</sup>‏ ‎‡9  1‏
919 ‎‡a  eshrepgtconsortiumgoodpracticerecommendationsforthedetectionofmonogenicdisorders‏ ‎‡A  ESHRE PGT Consortium good practice recommendations for the detection of monogenic disorders‏ ‎‡9  1‏
919 ‎‡a  evaluationofpcrbasedpreimplantationgeneticdiagnosisappliedtomonogenicdiseasesacollaborativeeshrepgdconsortiumstudy‏ ‎‡A  Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study.‏ ‎‡9  1‏
919 ‎‡a  expressionofstemcellmarkersoct4kititga6anditgb1inthemalegerminalepithelium‏ ‎‡A  Expression of stem cell markers: OCT4, KIT, ITGA6, and ITGB1 in the male germinal epithelium.‏ ‎‡9  1‏
919 ‎‡a  geneticregulationonexvivodifferentiatednaturalkillercellsfromhumanumbilicalcordbloodcd34+cells‏ ‎‡A  Genetic regulation on ex vivo differentiated natural killer cells from human umbilical cord blood CD34+ cells‏ ‎‡9  1‏
919 ‎‡a  characterizationofmissensemutationsandlargedeletionsinthealplgenebysequencingandquantitativemultiplexpcrofshortfragments‏ ‎‡A  Characterization of missense mutations and large deletions in the ALPL gene by sequencing and quantitative multiplex PCR of short fragments.‏ ‎‡9  1‏
919 ‎‡a  characterizationofcysticfibrosisconductancetransmembraneregulatorgenemutationsandivs8polytvariantsinportuguesepatientswithcongenitalabsenceofthevasdeferens‏ ‎‡A  Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens‏ ‎‡9  1‏
919 ‎‡a  genomicimprintingindisruptivespermatogenesis‏ ‎‡A  Genomic imprinting in disruptive spermatogenesis‏ ‎‡9  1‏
919 ‎‡a  humanspermatogenicfailurepurgesdeleteriousmutationloadfromtheautosomesandbothsexchromosomesincludingthegenedmrt1‏ ‎‡A  Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.‏ ‎‡9  1‏
919 ‎‡a  immunohistochemicalstudyoftheexpressionofmuc6mucinandcoexpressionofothersecretedmucins‏ ‎‡A  Immunohistochemical study of the expression of MUC6 mucin and co-expression of other secreted mucins‏ ‎‡9  1‏
919 ‎‡a  immunohistochemicalstudyoftheexpressionofmuc6mucinandcoexpressionofothersecretedmucinsmuc5acandmuc2inhumangastriccarcinomas‏ ‎‡A  Immunohistochemical study of the expression of MUC6 mucin and co-expression of other secreted mucins (MUC5AC and MUC2) in human gastric carcinomas‏ ‎‡9  1‏
919 ‎‡a  characterizationofcysticfibrosisconductancetransmembraneregulatorgenemutationsandivs8poly‏ ‎‡A  Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly‏ ‎‡9  1‏
919 ‎‡a  biallelicrecessivelossoffunctionvariantsinfancmcausenonobstructiveazoospermia‏ ‎‡A  Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia‏ ‎‡9  1‏
919 ‎‡a  azfanddazgenecopyspecificdeletionanalysisinmaturationarrestandsertolicellonlysyndrome‏ ‎‡A  AZF and DAZ gene copy-specific deletion analysis in maturation arrest and Sertoli cell-only syndrome‏ ‎‡9  1‏
919 ‎‡a  keratitisichthyosisdeafnesssyndromecausedbygjb2maternalmosaicism‏ ‎‡A  Keratitis-Ichthyosis-Deafness Syndrome Caused by GJB2 Maternal Mosaicism‏ ‎‡9  1‏
919 ‎‡a  methylationdefectsofimprintedgenesinhumantesticularspermatozoa‏ ‎‡A  Methylation defects of imprinted genes in human testicular spermatozoa‏ ‎‡9  1‏
919 ‎‡a  molecularandfunctionalcharacterizationofcbavdcausingmutationslocatedincftrnucleotidebindingdomains‏ ‎‡A  Molecular and functional characterization of CBAVD-causing mutations located in CFTR nucleotide-binding domains‏ ‎‡9  1‏
919 ‎‡a  associationofcysticfibrosisgeneticmodifierswithcongenitalbilateralabsenceofthevasdeferens‏ ‎‡A  Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens‏ ‎‡9  1‏
919 ‎‡a  molecularcharacterizationofthecysticfibrosistransmembraneconductanceregulatorgeneincongenitalabsenceofthevasdeferens‏ ‎‡A  Molecular characterization of the cystic fibrosis transmembrane conductance regulator gene in congenital absence of the vas deferens‏ ‎‡9  1‏
919 ‎‡a  muc1genepolymorphismandgastriccanceranepidemiologicalstudy‏ ‎‡A  MUC1 gene polymorphism and gastric cancer--an epidemiological study.‏ ‎‡9  1‏
919 ‎‡a  aneuploidiesdetectioninmiscarriagesandfetaldeathsusingmultiplexligationdependentprobeamplificationanalternativeforspeedingupresults‏ ‎‡A  Aneuploidies Detection in Miscarriages and Fetal Deaths Using Multiplex Ligation-Dependent Probe Amplification: An Alternative for Speeding up Results?‏ ‎‡9  1‏
919 ‎‡a  muc1genepolymorphisminthegastriccarcinogenesispathway‏ ‎‡A  MUC1 gene polymorphism in the gastric carcinogenesis pathway.‏ ‎‡9  1‏
919 ‎‡a  muc1polymorphismconfersincreasedriskforintestinalmetaplasiainacolombianpopulationwithchronicgastritis‏ ‎‡A  MUC1 polymorphism confers increased risk for intestinal metaplasia in a Colombian population with chronic gastritis‏ ‎‡9  1‏
919 ‎‡a  muc6genepolymorphisminhealthyindividualsandingastriccancerpatientsfromnorthernportugal‏ ‎‡A  MUC6 gene polymorphism in healthy individuals and in gastric cancer patients from northern Portugal.‏ ‎‡9  1‏
919 ‎‡a  mucinsandmucinassociatedcarbohydrateantigensexpressioningastriccarcinomacelllines‏ ‎‡A  Mucins and mucin-associated carbohydrate antigens expression in gastric carcinoma cell lines‏ ‎‡9  1‏
919 ‎‡a  novelhumanpathologicalmutationsgenesymbolgladiseasefabrydisease‏ ‎‡A  Novel human pathological mutations. Gene symbol: GLA. Disease: Fabry disease‏ ‎‡9  1‏
919 ‎‡a  applicationoftouchfishinthestudyofmosaictetraploidyandmaternalcellcontaminationinpregnancylosses‏ ‎‡A  Application of touch FISH in the study of mosaic tetraploidy and maternal cell contamination in pregnancy losses‏ ‎‡9  1‏
919 ‎‡a  phenotypicexpressioninthe1caseofcompletetrisomy12combinationofprenatalultrasoundandnecropsicexamination‏ ‎‡A  Phenotypic expression in the first case of complete trisomy 12: combination of prenatal ultrasound and necropsic examination‏ ‎‡9  1‏
919 ‎‡a  quantitativeanalysisofcellularproliferationanddifferentiationofthehumanseminiferousepitheliuminvitro‏ ‎‡A  Quantitative analysis of cellular proliferation and differentiation of the human seminiferous epithelium in vitro‏ ‎‡9  1‏
919 ‎‡a  raredoublesexandmab3relatedtranscriptionfactor1regulatoryvariantsinseverespermatogenicfailure‏ ‎‡A  Rare double sex and mab-3-related transcription factor 1 regulatory variants in severe spermatogenic failure‏ ‎‡9  1‏
919 ‎‡a  relevanceofgenomicimprintinginintrauterinehumangrowthexpressionofcdkn1ch19igf2kcnq1andphlda2imprintedgenes‏ ‎‡A  Relevance of genomic imprinting in intrauterine human growth expression of CDKN1C, H19, IGF2, KCNQ1 and PHLDA2 imprinted genes‏ ‎‡9  1‏
919 ‎‡a  semenqualityisaffectedbyhlaclass1allelestogetherwithsexuallytransmitteddiseases‏ ‎‡A  Semen quality is affected by HLA class I alleles together with sexually transmitted diseases‏ ‎‡9  1‏
919 ‎‡a  sequencediversityattheproximal14q321serpinsubclusterevidencefornaturalselectionfavoringthepseudogenizationofserpina2‏ ‎‡A  Sequence diversity at the proximal 14q32.1 SERPIN subcluster: evidence for natural selection favoring the pseudogenization of SERPINA2.‏ ‎‡9  1‏
919 ‎‡a  sequencevariationatklkandwfdcclustersanditsassociationtosemenhyperviscosityandothermaleinfertilityphenotypes‏ ‎‡A  Sequence variation at KLK and WFDC clusters and its association to semen hyperviscosity and other male infertility phenotypes‏ ‎‡9  1‏
919 ‎‡a  spectrumofcftrgenesequencevariantsinanorthernportugalpopulation‏ ‎‡A  Spectrum of CFTR gene sequence variants in a northern Portugal population‏ ‎‡9  1‏
919 ‎‡a  uniquey13translocationinamalewitholigozoospermiacytogeneticandmolecularstudies‏ ‎‡A  Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies‏ ‎‡9  1‏
919 ‎‡a  clinicalutilityofpgdwithhlamatchingacollaborativemulticentreeshrestudy‏ ‎‡A  The clinical utility of PGD with HLA matching: a collaborative multi-centre ESHRE study‏ ‎‡9  1‏
919 ‎‡a  g1170ctpolymorphismofthe5untranslatedregionofthehumanalphagalactosidasegeneisassociatedwithdecreasedenzymeexpressionevidencefromafamilystudy‏ ‎‡A  The g.1170C>T polymorphism of the 5' untranslated region of the human alpha-galactosidase gene is associated with decreased enzyme expression--evidence from a family study‏ ‎‡9  1‏
919 ‎‡a  mutationalspectrumofwt1inmaleinfertility‏ ‎‡A  The mutational spectrum of WT1 in male infertility.‏ ‎‡9  1‏
919 ‎‡a  treatmentbytesticularspermextractionandintracytoplasmicsperminjectionof65azoospermicpatientswithnonmosaicklinefeltersyndromewithbirthof17healthychildren‏ ‎‡A  Treatment by testicular sperm extraction and intracytoplasmic sperm injection of 65 azoospermic patients with non-mosaic Klinefelter syndrome with birth of 17 healthy children‏ ‎‡9  1‏
996 ‎‡2  PTBNP|191253‏
996 ‎‡2  ISNI|0000000371174780‏
996 ‎‡2  PTBNP|1587207‏
996 ‎‡2  ISNI|0000000067226179‏
996 ‎‡2  ISNI|0000000069314412‏
996 ‎‡2  SUDOC|229066461‏
996 ‎‡2  ISNI|0000000069812972‏
996 ‎‡2  RERO|A023169332‏
996 ‎‡2  LC|n 94076710‏
996 ‎‡2  PTBNP|1569967‏
996 ‎‡2  PTBNP|243467‏
996 ‎‡2  PTBNP|180600‏
996 ‎‡2  PTBNP|1778877‏
996 ‎‡2  ISNI|0000000069301304‏
996 ‎‡2  PTBNP|1206333‏
996 ‎‡2  LC|n 81044458‏
996 ‎‡2  ISNI|0000000066402695‏
996 ‎‡2  ISNI|0000000081801328‏
996 ‎‡2  PTBNP|37909‏
996 ‎‡2  PTBNP|1479397‏
996 ‎‡2  PTBNP|1348578‏
996 ‎‡2  ISNI|0000000068996503‏
996 ‎‡2  SUDOC|241028280‏
996 ‎‡2  PTBNP|1738055‏
996 ‎‡2  NTA|109608763‏
996 ‎‡2  ISNI|0000000068989792‏
996 ‎‡2  ISNI|0000000070420044‏
996 ‎‡2  ISNI|0000000067123823‏
996 ‎‡2  NSK|000539326‏
996 ‎‡2  PTBNP|1855023‏
996 ‎‡2  DNB|1155858891‏
996 ‎‡2  PTBNP|1345540‏
996 ‎‡2  LC|n 2012039050‏
996 ‎‡2  ISNI|0000000068193962‏
996 ‎‡2  ISNI|0000000393528789‏
996 ‎‡2  PTBNP|1472678‏
996 ‎‡2  PTBNP|1367219‏
996 ‎‡2  SIMACOB|430926339‏
996 ‎‡2  PTBNP|1470209‏
996 ‎‡2  PTBNP|1926598‏
996 ‎‡2  DNB|1157384412‏
996 ‎‡2  PTBNP|1611584‏
996 ‎‡2  PTBNP|203890‏
996 ‎‡2  PTBNP|233503‏
996 ‎‡2  PTBNP|122557‏
996 ‎‡2  ISNI|0000000068600345‏
997 ‎‡a  0 0 lived 0 0‏ ‎‡9  1‏