6533b834fe1ef96bd129cdff
RESEARCH PRODUCT
Susceptibility to Heart Defects in Down Syndrome Is Associated with Single Nucleotide Polymorphisms in HAS 21 Interferon Receptor Cluster and VEGFA Genes
Letizia ScolaClaudia Leonarda AmmoscatoRosa Maria GiarratanaTiziana FragapaneDomenico LioMaria PiccioneCarmela Rita Balistrerisubject
0301 basic medicineVEGFAAdultHeart Defects CongenitalMaleVascular Endothelial Growth Factor ADown syndromelcsh:QH426-470AdolescentChromosomes Human Pair 21Down syndromeSNPSingle-nucleotide polymorphismBiologyPolymorphism Single NucleotideArticle03 medical and health sciencesHeart disorder0302 clinical medicineGenotypeGeneticsmedicineHumansGeneGenetics (clinical)IFNRReceptors InterferonGeneticsmedicine.diseasePhenotypeHeart defectlcsh:GeneticsVascular endothelial growth factor A030104 developmental biologySettore MED/03 - Genetica Medica030220 oncology & carcinogenesisMultigene Familyheart defectsFemaleChromosome 21SNPsdescription
Background: Congenital heart defects (CHDs) are present in about 40&ndash
year | journal | country | edition | language |
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2020-11-28 | Genes |