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Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience

PaperCitations, authors & open-access status

Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience have?

ScholarIQcitation count

Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience has 19 citations in the OpenAlex counts ScholarIQ stores.

When was Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience published?

ScholarIQyear

Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience has 2022 year in the ScholarIQ index.

What is the open-access status of Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience?

ScholarIQoa status

Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience has gold oa status in the ScholarIQ index.

What is the DOI of Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience?

ScholarIQdoi

The DOI for Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience is on the source record.

What is the PMID of Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience?

ScholarIQpmid

The PMID for Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience is on the source record.

What is the OpenAlex record for Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience?

ScholarIQopenalex

The OpenAlex for Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience is on the source record.

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