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Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome

Wellcome Open Research(2020)10.12688/wellcomeopenres.15465.2Source: DataRank Database

Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome is a research paper published in Wellcome Open Research (2020). On theSindex it has a DataRank of 0. It has been cited 11 times.

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Open Access11 citations

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Enrichment:Funding (3 grants)OA: goldTopics (4)IDs (PubMed, PMC)Annotations (1)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (22)

Senthil Senniappan ORCID,Thomas W. Laver ORCID,Richard Caswell ORCID,Martin Zenker ORCID,Klaus Mohnike ORCID

Live enrichment

PubMed:32832699 PMC:PMC7422856

Wellcome Trust

Grant: 105636

Wellcome Trust

Grant: 105636/Z/14/Z

Wellcome Trust

goldLicense: cc-by

publisherhttps://wellcomeopenresearch.org/articles/4-149/v2/pdf

publisherhttps://wellcomeopenresearch.org/articles/4-149/v2/xml

publisherhttps://wellcomeopenresearch.org/articles/4-149/v2/iparadigms

repositoryhttps://doaj.org/article/d2f10b46905b437e918ce37dd11757b4

repositoryhttps://figshare.com/articles/journal_contribution/Refinement_of_the_critical_genomic_region_for_congenital_hyperinsulinism_in_the_Chromosome_9p_deletion_syndrome/29773199

Keywords

Chromosome 9pHyperinsulinismhypoglycaemiaDeletions

Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome

FAIR Checklist

Authors (22)

Funding (3 grants)

Open Access

Topics

Annotations (Europe PMC)