VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q86417737 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241221010741.0
008 241221nneanz||abbn n and d
035 ‎‡a (WKP)Q86417737‏
024 ‎‡a 0000-0001-8616-9138‏ ‎‡2 orcid‏
035 ‎‡a (OCoLC)Q86417737‏
100 0 ‎‡a মাইকেল এফ মারি‏ ‎‡c গবেষক‏ ‎‡9 bn‏
375 ‎‡a 1‏ ‎‡2 iso5218‏
400 0 ‎‡a Michael F Murray‏ ‎‡c researcher‏ ‎‡9 en‏
400 0 ‎‡a Michael F Murray‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
670 ‎‡a Author's COVID-19 outcomes and the human genome‏
670 ‎‡a Author's Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study‏
670 ‎‡a Author's Parental attitudes and expectations towards receiving genomic test results in healthy children.‏
670 ‎‡a Author's Parental DNA sequence is critical family history in clinical genomics.‏
670 ‎‡a Author's Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine Experience‏
670 ‎‡a Author's The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research.‏
670 ‎‡a Author's Your DNA is not your diagnosis: getting diagnoses right following secondary genomic findings.‏
909 ‎‡a (orcid) 0000000186169138‏ ‎‡9 1‏
919 ‎‡a yourdnaisnotyourdiagnosisgettingdiagnosesrightfollowingsecondarygenomicfindings‏ ‎‡A Your DNA is not your diagnosis: getting diagnoses right following secondary genomic findings.‏ ‎‡9 1‏
919 ‎‡a geisingermycodecommunityhealthinitiativeanelectronichealthrecordlinkedbiobankforprecisionmedicineresearch‏ ‎‡A The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research.‏ ‎‡9 1‏
919 ‎‡a patientcenteredprecisionhealthinalearninghealthcaresystemgeisingersgenomicmedicineexperience‏ ‎‡A Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine Experience‏ ‎‡9 1‏
919 ‎‡a parentaldnasequenceiscriticalfamilyhistoryinclinicalgenomics‏ ‎‡A Parental DNA sequence is critical family history in clinical genomics.‏ ‎‡9 1‏
919 ‎‡a parentalattitudesandexpectationstowardsreceivinggenomictestresultsinhealthychildren‏ ‎‡A Parental attitudes and expectations towards receiving genomic test results in healthy children.‏ ‎‡9 1‏
919 ‎‡a distributionandclinicalimpactoffunctionalvariantsin50726wholeexomesequencesfromthediscovehrstudy‏ ‎‡A Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study‏ ‎‡9 1‏
919 ‎‡a covid19outcomesandthehumangenome‏ ‎‡A COVID-19 outcomes and the human genome‏ ‎‡9 1‏
946 ‎‡a b‏ ‎‡9 1‏
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996 ‎‡2 LC|no2019185719‏
996 ‎‡2 LC|n 86105556‏
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996 ‎‡2 NLA|000035756011‏
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996 ‎‡2 LNB|LNC10-000134686‏
996 ‎‡2 BNF|12134486‏
996 ‎‡2 J9U|987008914549405171‏
996 ‎‡2 DNB|170661709‏
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996 ‎‡2 CAOONL|ncf11369076‏
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996 ‎‡2 NTA|327194529‏
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996 ‎‡2 RERO|A003620017‏
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996 ‎‡2 CAOONL|ncf10289258‏
996 ‎‡2 BNF|12408841‏
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996 ‎‡2 LNB|LNC10-000060575‏
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996 ‎‡2 CAOONL|ncf11590874‏
996 ‎‡2 VLACC|000045842‏
996 ‎‡2 LIH|LNB:B_l_0_f_;=B_k_‏
997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏
998 ‎‡a Murray, Michael F.‏ ‎‡c (médecin)‏ ‎‡2 CAOONL|ncf10724613‏ ‎‡3 title: (0.65, 'clinicalgenomics', 'parentaldnasequenceiscriticalfamilyhistoryinclinicalgenomics')‏
998 ‎‡a Murray, Michael F.‏ ‎‡c (Physician)‏ ‎‡2 J9U|987007328297905171‏ ‎‡3 viafid‏
998 ‎‡a Murray, Michael F.‏ ‎‡c (Physician)‏ ‎‡2 LC|nb2014001376‏ ‎‡3 title: (0.65, 'clinicalgenomics', 'parentaldnasequenceiscriticalfamilyhistoryinclinicalgenomics')‏
998 ‎‡a Murray, Michael F.‏ ‎‡2 NUKAT|n 2016011896‏ ‎‡3 viafid‏