Adès, Lesley C.
The University of Sydney · The University of Melbourne · Children's Hospital at Westmead · Victorian Clinical Genetics Services · Monash Health · Sydney Children’s Hospitals Network · Murdoch Children's Research Institute
2 papers on CoChat
Most cited papers
- Verified
Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System
Australian Genomics Health Alliance Acute Care Flagship, Lunke, S., Eggers, S., Wilson, M., Patel, C., Barnett, C. P., Pinner, J., Sandaradura, S. A., Buckley, M. F., Krzesinski, E. I., et al. (2020) · JAMA
Genomics and Rare DiseasesMetabolism and Genetic Disorders
Cited by 239
- Verified
Novel Types of Mutation Responsible for the Dermatosparactic Type of Ehlers–Danlos Syndrome (Type VIIC) and Common Polymorphisms in the ADAMTS2 Gene
Colige, A., Nuytinck, L., Hausser, I., van Essen, A. J., Thiry, M., Herens, C., Adès, L. C., Malfait, F., Paepe, A. D., Franck, P., et al. (2004) · Journal of Investigative Dermatology
Connective tissue disorders researchProtease and Inhibitor Mechanisms
Cited by 139
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