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/vufind/Search/Results?lookfor=%22Bartram%2C+Claus+R.%22&type=Person&sort=year
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PubPharm (363)
1
Genetic Variation in ABCC4 and CFTR and Acute Pancreatitis during Treatment of Pediatric Acute Lymphoblastic Leukemia
enthalten in:
Journal of clinical medicine
| 2021
von
Bartram, T.
|
Schütte, P.
|
Möricke, A.
| +16
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2
Genetic Variation in ABCC4 and CFTR and Acute Pancreatitis during Treatment of Pediatric Acute Lymphoblastic Leukemia
sonderdruck aus:
Journal of Clinical Medicine
| 20 October 2021
von
Bartram, T.
|
Schütte, P.
|
Möricke, A.
| +16
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3
Genetic variation in ABCC4 and CFTR and acute pancreatitis during treatment of pediatric acute lymphoblastic leukemia
enthalten in:
Journal of Clinical Medicine
| 20 October 2021
von
Bartram, T.
|
Schütte, P.
|
Möricke, A.
| +16
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4
Breast cancer risk in BRCA1/2 mutation carriers and noncarriers under prospective intensified surveillance
enthalten in:
International journal of cancer
| 2020
von
Engel, C.
|
Fischer, C.
|
Zachariae, S.
| +36
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5
Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk
enthalten in:
Nature communications
| 2019
von
Vijayakrishnan, J.
|
Qian, M.
|
Studd, J.
| +23
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6
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants : An ENIGMA resource to support clinical variant classification
enthalten in:
Human mutation
| 2019
von
Parsons, M.
|
Tudini, E.
|
Li, H.
| +99
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7
Identification and prioritisation of causal variants in human genetic disorders from exome or whole genome sequencing data
enthalten in:
bioRxiv.org
| 2019
von
Paramasivam, N.
|
Granzow, M.
|
Evers, C.
| +5
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8
The Frog Xenopus as a Model to Study Joubert Syndrome : The Case of a Human Patient With Compound Heterozygous Variants in PIBF1
enthalten in:
Frontiers in physiology
| 2019
von
Ott, T.
|
Kaufmann, L.
|
Granzow, M.
| +9
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9
Author Correction : Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia
enthalten in:
Nature communications
| 2019
von
Vijayakrishnan, J.
|
Studd, J.
|
Broderick, P.
| +93
ErratumFor: Nat Commun. 2018 Apr 9;9(1):1340. - PMID 29632299
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10
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants : An ENIGMA resource to support clinical variant classification
enthalten in:
Human mutation
| 2019
von
Parsons, M.
|
Tudini, E.
|
Li, H.
| +218
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