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- 2022
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Mark
Multiple sclerosis diagnosis and phenotype identification by multivariate classification of in vivo frontal cortex metabolite profiles
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- Contribution to journal › Article
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Mark
Life histories as mosaics : Plastic and genetic components differ among traits that underpin life-history strategies
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- Contribution to journal › Article
- 2021
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Mark
Congenital stationary night blindness : an update and review of the disease spectrum in Saudi Arabia
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- Contribution to journal › Scientific review
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Mark
Synovial fluid neutrophils in oligoarticular juvenile idiopathic arthritis have an altered phenotype and impaired effector functions
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- Contribution to journal › Article
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Mark
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
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- Contribution to journal › Article
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Mark
Treatment outcomes in persons with severe haemophilia B in the Nordic region : The B-NORD study
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- Contribution to journal › Article
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Mark
AXL Knock-Out in SNU475 Hepatocellular Carcinoma Cells Provides Evidence for Lethal Effect Associated with G2 Arrest and Polyploidization
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- Contribution to journal › Article
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Mark
The European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI)-clinical phenotypes and their predictors based on a cohort of 1000 patients
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- Contribution to journal › Article
- 2020
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Mark
Myoclonus-dystonia (DYT11, DYT-SGCE) - a channelopathy?
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- Contribution to journal › Debate/Note/Editorial
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Mark
Recurrent Fusions Between YAP1 and KMT2A in Morphologically Distinct Neoplasms Within the Spectrum of Low-grade Fibromyxoid Sarcoma and Sclerosing Epithelioid Fibrosarcoma
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- Contribution to journal › Article