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Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature

PaperCitations, authors & open-access status

Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature is a paper indexed in PICO Portal from OpenAlex.

How many citations does Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature have?

PICO Portalcitation count

Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature has 94 citations in the OpenAlex counts PICO Portal stores.

When was Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature published?

PICO Portalyear

Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature has 2020 year in the PICO Portal index.

What is the open-access status of Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature?

PICO Portaloa status

Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature has green oa status in the PICO Portal index.

What is the DOI of Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature?

PICO Portaldoi

The DOI for Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature is on the source record.

What is the PMID of Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature?

PICO Portalpmid

The PMID for Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature is on the source record.

What is the OpenAlex record for Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature?

PICO Portalopenalex

The OpenAlex for Natural history of Ollier disease and Maffucci syndrome: Patient survey and review of clinical literature is on the source record.

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