A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
University of Washington · Signature Research (United States) · +26 more institutions
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Abstract
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Citation impact
673
total citations
- FWCI
- 55.22
- Percentile
- 100%
- References
- 50
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Authors
59Topics & keywords
Topics
Keywords
- Proband
- Phenotype
- Biology
- Genetics
- Microdeletion syndrome
- Mutation
- Disease
- Bioinformatics
UN Sustainable Development Goals
- Good health and well-being
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