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American Journal of Medical Genetics. Part A|November 15, 2006
Clinical features and management issues in Mowat-Wilson syndromeMargaret P Adam, Susan Schelley, Renata Gallagher, et al.Journal of Craniofacial Genetics and Developmental Biology|December 10, 1999
Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutationS Beiraghi, A Miller-Chisholm, W J Kimberling, et al.Nucleic Acids Research|November 9, 2019
The Monarch Initiative in 2019: an integrative data and analytic platform connecting phenotypes to genotypes across speciesKent A Shefchek, Nomi L Harris, Michael Gargano, et al.Nucleic Acids Research|November 27, 2018
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resourcesSebastian Köhler, Leigh Carmody, Nicole Vasilevsky, et al.Pageof 7