Bartram, Claus R. 1952-
Bartram, C. R.
Bartram, Claus R.
Claus Rainer Bartram
VIAF ID: 102380354 (Personal)
Permalink: http://viaf.org/viaf/102380354
Preferred Forms
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200 _ |
‡a
Bartram
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Claus R.
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100 1 _
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Bartram, C. R.
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100 1 _
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Bartram, C. R.
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100 1 _
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Bartram, C. R.
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100 1 _ ‡a Bartram, Claus R.
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100 1 _ ‡a Bartram, Claus R.
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100 1 _
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Bartram, Claus R.
‡d
1952-
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100 1 _
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Bartram, Claus R.
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1952-
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100 0 _
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Claus Rainer Bartram
4xx's: Alternate Name Forms (16)
5xx's: Related Names (7)
- 510 2 _
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Deutsche Akademie der Naturforscher Leopoldina
‡4
affi
‡4
https://d-nb.info/standards/elementset/gnd#affiliation
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Affiliation
- 551 _ _
‡a
Heidelberg
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ortw
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https://d-nb.info/standards/elementset/gnd#placeOfActivity
- 510 2 _
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Institut für Humangenetik und Anthropologie
- 510 2 _
‡a
Ulm, Universiẗat
- 510 2 _
‡a
Universität Heidelberg
‡b
Institut für Humangenetik und Anthropologie
‡4
affi
‡4
https://d-nb.info/standards/elementset/gnd#affiliation
‡e
Affiliation
- 510 2 _
‡a
Universität Heidelberg
- 510 2 _
‡a
Universität Heidelberg. Marsilius-Kolleg
Works
| Title | Sources |
|---|---|
| Aus- und Weiterbildung in der klinischen Medizin Didaktik und Ausbildungskonzepte ; mit 13 Tabellen |
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| DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome |
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| Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy |
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| Frequent and sex-biased deletion of SLX4IP by illegitimate V(D)J-mediated recombination in childhood acute lymphoblastic leukemia |
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| Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study |
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| Genetic Variation in ABCC4 and CFTR and Acute Pancreatitis during Treatment of Pediatric Acute Lymphoblastic Leukemia |
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| Humangenetische Diagnostik : wissenschaftliche Grundlagen und gesellschaftliche Konsequenzen |
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| Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity |
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| Impact of clinical exomes in neurodevelopmental and neurometabolic disorders |
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| Loss of function of PGAP1 as a cause of severe encephalopathy identified by whole exome sequencing: lessons of the bioinformatics pipeline |
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| Menschenbilder und Wissenschaftskulturen, c2011: |
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| Molekulargenetische Charakterisierung von Leukämien des Menschen |
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| Next-generation personalised medicine for high-risk paediatric cancer patients – the INFORM pilot study |
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| Oncogenes in cancer diagnosis |
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| So rare we need to hunt for them: reframing the ethical debate on incidental findings |
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| Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort |
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| undurchsichtige Mensch |
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| Vererbung und Milieu |
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| Wider die Natur |
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