Inherited deletion of 9p22.3‐p24.3 and duplication of 18p11.31‐p11.32 associated with neurodevelopmental delay: Phenotypic matching of involved genes is a research paper published in Journal of Cellular and Molecular Medicine (2023). On theSindex it has a DataRank of 0. It has been cited 6 times.
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National Institutes of Health
Grant: 5U24HG011449-05
The Human Phenotype Ontology: Accelerating Computational Integration of Clinical Data for Genomics
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