Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation
Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation is a paper indexed in ScholarIQ from OpenAlex.
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Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation has 10 citations in the OpenAlex counts ScholarIQ stores.
When was Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation published?
Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation has 2017 year in the ScholarIQ index.
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Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation has closed oa status in the ScholarIQ index.
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