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- 2023
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Mark
The Swedish COG6-CDG experience and a comprehensive literature review
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- Contribution to journal › Article
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Mark
Manganese efflux transporter SLC30A10 missense polymorphism T95I associated with liver injury retains manganese efflux activity
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- Contribution to journal › Article
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Mark
A phenome-wide comparative analysis of genetic discordance between obesity and type 2 diabetes
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- Contribution to journal › Article
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Mark
HNF1B variant without hyperglycaemia as a cause of isolated profound hypomagnesaemia
(
- Contribution to journal › Article
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Mark
Genome-wide analysis of KMT2A-rearranged leukemia
2023) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
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Mark
Type 2 diabetes candidate genes, including PAX5, cause impaired insulin secretion in human pancreatic islets
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- Contribution to journal › Article
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Mark
Evaluation of genetic demultiplexing of single-cell sequencing data from model species
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- Contribution to journal › Article
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Acquired uniparental isodisomies involving chromosome 12 in paediatric B-cell precursor acute lymphoblastic leukaemia : Associations with chromosome 21 gains and SH2B3 mutations
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- Contribution to journal › Article
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Reduced binding of apoE4 to complement factor H promotes amyloid-β oligomerization and neuroinflammation
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- Contribution to journal › Article
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Mark
Rare-variant collapsing analyses of arterial hypertension in the UK biobank
(
- Contribution to journal › Letter