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Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation
PaperCitations, authors & open-access status
Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 10 citations, 2017 year and closed oa status.
10
Citations
2017
Year
closed
OA Status