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Cri du Chat Syndrome and Primary Ciliary Dyskinesia: A Common Genetic Cause on Chromosome 5p

UNC Libraries(2020)10.17615/q665-8329Source: DataRank Database

Cri du Chat Syndrome and Primary Ciliary Dyskinesia: A Common Genetic Cause on Chromosome 5p is a research paper published in UNC Libraries (2020). On theSindex it has a DataRank of 0.

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Open Access0 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (4 grants)Impact (FWCI 0.00)OA: greenTopics (32)IDs (PubMed, OpenAlex)SDGs (3)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (8)

Margaret Rosenfeld ORCID,Karen E. Weck ORCID,Margaret W. Leigh ORCID,Michael R. Knowles ORCID,Maimoona A. Zariwala ORCID

Live enrichment

PubMed:19910364 OpenAlex:https://openalex.org/W4298501920

National Institutes of Health

Grant: 8UL1TR000083-05

UNC Clinical and Translational Science Award

National Institutes of Health

Grant: 3UL1TR000423-07S1

Institute of Translational Health Sciences

National Institutes of Health

Grant: 5U54HL096458-14

Genetic Disorder of Mucocilary Clearance

National Institutes of Health

Grant: 5R01HL071798-04

Pathogenesis of PCD Lung Disease

FWCI

0.00

Citation Percentile

0.2%

greenLicense: Elsevier TDM

repositoryhttps://doi.org/10.17615/q665-8329

https://doi.org/10.1016/j.jpeds.2014.06.048

https://cdr.lib.unc.edu/downloads/qv33s482f

https://dx.doi.org/10.17615/q665-8329

https://pubmed.ncbi.nlm.nih.gov/25066065

Fields of Study

Genomic variations and chromosomal abnormalitiesChromosomal and Genetic VariationsGenetics and Neurodevelopmental Disorders0301 basic medicine0303 health sciences03 medical and health sciences

Keywords

Primary ciliary dyskinesiaChromosomeBiologyPrimary (astronomy)GeneticsMedicineInternal medicineGenePhysicsAstronomyCri-du-Chat SyndromeHemizygoteMaleKartagener SyndromeChromosome MappingAxonemal DyneinsRespiration DisordersRadiographyPhenotypeMutationChromosomes, Human, Pair 5HumansFemaleChromosome DeletionChildCodon

Sustainable Development Goals

SDG 3: 3. Good healthSDG 16: 16. Peace & justiceSDG 0: Zero hunger