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Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

PaperCitations, authors & open-access status

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis is a paper indexed in PICO Portal from OpenAlex.

How many citations does Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis have?

PICO Portalcitation count

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis has 577 citations in the OpenAlex counts PICO Portal stores.

When was Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis published?

PICO Portalyear

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis has 2010 year in the PICO Portal index.

What is the open-access status of Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis?

PICO Portaloa status

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis has green oa status in the PICO Portal index.

What is the DOI of Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis?

PICO Portaldoi

The DOI for Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis is on the source record.

What is the PMID of Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis?

PICO Portalpmid

The PMID for Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis is on the source record.

What is the OpenAlex record for Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis?

PICO Portalopenalex

The OpenAlex for Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis is on the source record.

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