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- 2023
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Mark
Identification of monogenic variants in more than ten per cent of children without type 1 diabetes-related autoantibodies at diagnosis in the Finnish Pediatric Diabetes Register
(
- Contribution to journal › Article
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Mark
An insulin hypersecretion phenotype precedes pancreatic β cell failure in MODY3 patient-specific cells
(
- Contribution to journal › Article
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Mark
Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine
(
- Contribution to journal › Scientific review
- 2022
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Mark
A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY
(
- Contribution to journal › Article
- 2020
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Mark
Human Physiology of Genetic Defects Causing Beta-cell Dysfunction
(
- Contribution to journal › Scientific review
- 2017
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Mark
Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance
(
- Contribution to journal › Article