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CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

PaperCitations, authors & open-access status

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language is a paper indexed in ScholarIQ from OpenAlex.

How many citations does CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language have?

ScholarIQcitation count

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language has 123 citations in the OpenAlex counts ScholarIQ stores.

When was CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language published?

ScholarIQyear

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language has 2018 year in the ScholarIQ index.

What is the open-access status of CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language?

ScholarIQoa status

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language has gold oa status in the ScholarIQ index.

What is the DOI of CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language?

ScholarIQdoi

The DOI for CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language is on the source record.

What is the PMID of CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language?

ScholarIQpmid

The PMID for CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language is on the source record.

What is the OpenAlex record for CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language?

ScholarIQopenalex

The OpenAlex for CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language is on the source record.

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