9 top medical experts on Chromosome 17p13.3 Duplication Syndrome across 1 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Chromosome 17p13.3 Duplication Syndrome: 17p13.3 microduplication syndrome is characterized by variable psychomotor delay and dysmorphic features.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
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