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1 |
WARS1 and SARS1: Two tRNA synthetases implicated in autosomal recessive microcephaly
Bögershausen, Nina. - Leipzig : Universitätsbibliothek Leipzig, 2025
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2 |
Evolutionary trajectories of small cell lung cancer under therapy
George, Julie. - Aachen : Universitätsbibliothek der RWTH Aachen, 2024
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3 |
Identifying blood-specific biomarkers for therapy-related clonal hematopoiesis in patients with hereditary or non-hereditary ovarian cancer
Weber-Lassalle, Konstantin. - Köln : Universitäts- und Stadtbibliothek Köln, 2022
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4 |
Prevalence of deleterious germline variants in risk genes including \(BRCA1/2\) in consecutive ovarian cancer patients (AGO-TR-1)
Harter, Philipp. - Würzburg : Universität Würzburg, 2022
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5 |
Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in BRCA1/2: results of the observational AGO-TR1 study (NCT02222883)
Hauke, Jan. - Kiel : Universitätsbibliothek Kiel, 2022
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6 |
Swarm Learning for decentralized and confidential clinical machine learning
Warnat-Herresthal, Stefanie. - Saarbrücken : Saarländische Universitäts- und Landesbibliothek, 2021
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7 |
Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in BRCA1/2: results of the observational AGO-TR1 study (NCT02222883)
Hauke, Jan. - Ulm : Universität Ulm, 2020
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8 |
Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech Development
Enthalten in Neuropediatrics Bd. 49, 2018, Nr. 06: 379-384
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9 |
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies
Pérez-Palma, Eduardo. - Frankfurt am Main : Universitätsbibliothek Johann Christian Senckenberg, 2017
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10 |
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies
Pérez-Palma, Eduardo. - Frankfurt am Main : Universitätsbibliothek Johann Christian Senckenberg, 2017
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