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- 2022
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Mark
Population-scale analysis of common and rare genetic variation associated with hearing loss in adults
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- Contribution to journal › Article
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Mark
A BALB/c IGHV Reference Set, Defined by Haplotype Analysis of Long-Read VDJ-C Sequences From F1 (BALB/c x C57BL/6) Mice
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- Contribution to journal › Article
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Mark
Pre-operative exercise and pyrexia as modifying factors in malignant hyperthermia (MH)
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- Contribution to journal › Article
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Mark
Amplification of CDK4 and MDM2 : a detailed study of a high-risk neuroblastoma subgroup
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- Contribution to journal › Article
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Mark
Extended genetic diagnostics for children with profound sensorineural hearing loss by implementing massive parallel sequencing. Diagnostic outcome, family experience and clinical implementation
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- Contribution to journal › Article
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Mark
Germline Mutations in CIDEB and Protection against Liver Disease
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- Contribution to journal › Article
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Mark
Subtype and cell type specific expression of lncRNAs provide insight into breast cancer
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- Contribution to journal › Article
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Mark
Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease
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- Contribution to journal › Article
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Mark
Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci
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- Contribution to journal › Article
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Mark
DNA methylation profiling improves routine diagnosis of paediatric central nervous system tumours : A prospective population-based study
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- Contribution to journal › Article