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Article

Johnson, B., Lowe, G.C., Futterer, J. et al. (31 more authors) (2016) Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects. Haematologica. ISSN 0390-6078

Ashrafian, H., Docherty, L., Leo, V. et al. (22 more authors) (2010) A Mutation in the Mitochondrial Fission Gene Dnm1l Leads to Cardiomyopathy. PLoS Genetics, 6 (6). e1001000. ISSN 1553-7390

Carpenter, D., Ringrose, C., Leo, V. et al. (5 more authors) (2009) The role of CACNA1S in predisposition to malignant hyperthermia. BMC Medical Genetics , 10. ISSN 1471-2350

This list was generated on Sun Oct 13 18:56:10 2019 BST.