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Human Phenotype Ontology Annotations for Rare Congenital Conditions: Application to Arthrogryposis Multiplex Congenita.

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Bibliographic Details
Title: Human Phenotype Ontology Annotations for Rare Congenital Conditions: Application to Arthrogryposis Multiplex Congenita.
Authors: Nematollahi, Shahrzad1,2, shahrzad.nematollahi@mail.mcgill.ca, Hamdy, Reggie C.3,4, van Bosse, Harold5, Li, Joyce3, Blanshay‐Goldberg, Daniel3, de Vries, Johanna I. P.6, Dieterich, Klaus7, Filges, Isabel8, Bedard, Tanya9, Haendel, Melissa10, Torres, Monica Munoz10, Robinson, Peter N.11, Dahan‐Oliel, Noémi1,2
Source: American Journal of Medical Genetics. Part A; Aug2025, Vol. 197 Issue 8, p1-16, 16p
Database: Applied Science & Technology Source
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