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Dispelling myths about rare disease registry system development., , , , , , , , and . Source Code for Biology and Medicine, (2013)Correction: Dispelling myths about rare disease registry system development., , , , , , , , and . Source Code for Biology and Medicine, (2014)The Human Phenotype Ontology in 2021., , , , , , , , , and 41 other author(s). Nucleic Acids Res., 49 (Database-Issue): D1207-D1217 (2021)An evaluation of GPT models for phenotype concept recognition., , , , , , , and . CoRR, (2023)The Human Phenotype Ontology in 2017., , , , , , , , , and 49 other author(s). Nucleic Acids Res., 45 (Database-Issue): D865-D876 (2017)An evaluation of GPT models for phenotype concept recognition., , , , , , , and . BMC Medical Informatics Decis. Mak., 24 (1): 30 (December 2024)Modeling 3D Facial Shape from DNA, , , , , , , , , and 13 other author(s). PLOS Genetics, 10 (3): 1-14 (March 2014)Genotype-phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders, , , , , , , , , and 1 other author(s). medRxiv, (2020)Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources., , , , , , , , , and 59 other author(s). Nucleic Acids Res., 47 (Database-Issue): D1018-D1027 (2019)Automatic concept recognition using the Human Phenotype Ontology reference and test suite corpora., , , , , , , , , and . Database J. Biol. Databases Curation, (2015)