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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 PICO Portal from OpenAlex.

How many citations does Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation have?

PICO Portalcitation count

Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation has 10 citations in the OpenAlex counts PICO Portal stores.

When was Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation published?

PICO Portalyear

Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation has 2017 year in the PICO Portal index.

What is the open-access status of Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation?

PICO Portaloa status

Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation has closed oa status in the PICO Portal index.

What is the DOI of Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation?

PICO Portaldoi

The DOI for Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation is on the source record.

What is the PMID of Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation?

PICO Portalpmid

The PMID for Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation is on the source record.

What is the OpenAlex record for Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation?

PICO Portalopenalex

The OpenAlex for Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation is on the source record.

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