Suchergebnisse - "DNA/ethics"
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1
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Genetics in Medicine. 21:2774-2780
Schlagwörter: Adult, 0301 basic medicine, DNA Copy Number Variations, DATABASE, Noninvasive Prenatal Testing, Sequence Analysis, DNA/ethics, DNA Copy Number Variations/genetics, 3105 Genetics, Noninvasive Prenatal Testing/ethics, DUCHENNE MUSCULAR-DYSTROPHY, Dystrophin, 03 medical and health sciences, Fetus, Pregnancy, Prenatal Diagnosis/ethics, Prenatal Diagnosis, Humans, DYSTROPHINOPATHY, Dystrophin/genetics, Genetics & Heredity, 0604 Genetics, Incidental Findings, 0303 health sciences, Science & Technology, 1103 Clinical Sciences, DNA, Sequence Analysis, DNA, 3. Good health, MODEL, fetus, NIPS, secondary findings, Female, pregnancy, Life Sciences & Biomedicine, DMD gene, maternal CNV
Zugangs-URL: https://www.nature.com/articles/s41436-019-0564-4.pdf
https://pubmed.ncbi.nlm.nih.gov/31197268
https://researchportal.vub.be/nl/publications/maternal-copy-number-variations-in-the-dmd-gene-as-secondary-find
https://www.nature.com/articles/s41436-019-0564-4.pdf
https://www.nature.com/articles/s41436-019-0564-4
https://www.ncbi.nlm.nih.gov/pubmed/31197268
https://biblio.vub.ac.be/vubir/maternal-copynumber-variations-in-the-dmd-gene-as-secondary-findings-in-noninvasive-prenatal-screening(e41bc943-5328-4d97-ab96-e75947fcd596).html -
2
Autoren: et al.
Weitere Verfasser: et al.
Quelle: The Journal of Pathology. 246:405-414
Schlagwörter: 0301 basic medicine, Genetic Privacy/ethics, Genetic Counseling, Sequence Analysis, DNA/ethics, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, molecular pathology, Predictive Value of Tests, Neoplasms, Journal Article, Biomarkers, Tumor, cancer, Humans, genetics, Genetic Predisposition to Disease, Pathology, Molecular, Practice Patterns, Physicians', Genetic Privacy, DNA, Neoplasm/genetics, Genetic Counseling/ethics, Pathologists/ethics, 0303 health sciences, Informed Consent, Reproducibility of Results, personalized medicine, DNA, Neoplasm, Sequence Analysis, DNA, Informed Consent/ethics, Pathology, Molecular/ethics, ethics, Neoplasms/genetics, 3. Good health, Pathologists, Guideline Adherence/ethics, Phenotype, Practice Guidelines as Topic, Practice Patterns, Physicians'/ethics, pathology, next-generation sequencing, Guideline Adherence, Biomarkers, Tumor/genetics
Dateibeschreibung: application/pdf
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/30125358
https://dspace.library.uu.nl/handle/1874/388470
https://europepmc.org/article/MED/30125358
https://jglobal.jst.go.jp/detail?JGLOBAL_ID=201802258422339550
https://www.ncbi.nlm.nih.gov/pubmed/30125358
https://www.narcis.nl/publication/RecordID/oai%3Adspace.library.uu.nl%3A1874%2F388470
https://onlinelibrary.wiley.com/doi/abs/10.1002/path.5157
https://dspace.library.uu.nl/handle/1874/388470 -
3
Autoren:
Schlagwörter: DNA, Ethics
Dateibeschreibung: application/pdf
Zugangs-URL: https://hdl.handle.net/1887/3718073
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4
Autoren: et al.
Quelle: Tidsskrift for Den Norske Laegeforening. 135(22):2031
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5
Autoren: Gaini, Shahin
Quelle: Ugeskrift for Laeger. 175(34):1903
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6
Autoren: et al.
Weitere Verfasser: et al.
Schlagwörter: genetics, pathology, next-generation sequencing, cancer, ethics, molecular pathology, personalized medicine, Predictive Value of Tests, Genetic Privacy/ethics, Humans, Neoplasms/genetics, Biomarkers, Tumor/genetics, Genetic Predisposition to Disease, Reproducibility of Results, Informed Consent/ethics, Pathologists/ethics, Practice Patterns, Physicians'/ethics, DNA, Neoplasm/genetics, Phenotype, Guideline Adherence/ethics, Genetic Counseling/ethics, Molecular/ethics, Sequence Analysis, DNA/ethics, Practice Guidelines as Topic, Pathology and Forensic Medicine, Journal Article
Dateibeschreibung: application/pdf
Verfügbarkeit: https://dspace.library.uu.nl/handle/1874/388470
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7
Autoren: Hertz, Jens Michael
Quelle: Ugeskrift for Laeger. 176(23):2151
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8
Autoren: Callier, Shawneequa L.
Quelle: Clinical Research and Leadership Faculty Publications
Schlagwörter: DNA--analysis, Education, Medical, Graduate--ethics, Pharmacy, Genetic Research--ethics, Genetic Testing--ethics, Nontherapeutic Human Experimentation--ethics, Polymorphism, Single Nucleotide, Sequence Analysis, DNA--ethics, Students, Universities--ethics, Medicine and Health Sciences
Relation: https://hsrc.himmelfarb.gwu.edu/smhs_crl_facpubs/3; http://www.ncbi.nlm.nih.gov/pubmed?holding=dcgwulib_fft_ndi&dr=abstract&otool=dcgwulib&term=22452475
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9
Autoren: Gaini, Shahin
Quelle: Ugeskrift for Laeger. 175(12):836
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10
Autoren:
Quelle: Tidsskrift for Den Norske Laegeforening. 132(19):2190
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11
Autoren: By:Sacha Pfeiffer, GLOBE STAFF
Quelle: Boston Globe, January 25, 2000 Metro/Region THIRD, 2pp
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12
Autoren: et al.
Quelle: Clinical genetics [Clin Genet] 2015 Apr; Vol. 87 (4), pp. 301-10. Date of Electronic Publication: 2014 Oct 07.
Publikationsart: Journal Article; Research Support, Non-U.S. Gov't; Review
Info zur Zeitschrift: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
MeSH-Schlagworte: Incidental Findings*, Disclosure/*ethics , Genetic Testing/*methods , Guidelines as Topic/*standards, Adult ; Age of Onset ; Child ; Genetic Testing/ethics ; Humans ; Minors ; Predictive Value of Tests ; Sequence Analysis, DNA/methods
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