Cornelia De Lange Syndrome: Disease Bioinformatics
Research of Cornelia De Lange Syndrome has been linked to Congenital Abnormality, Cytogenetic Abnormality, Growth Retardation, Microcephaly, Trisomy. The study of Cornelia De Lange Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Cornelia De Lange Syndrome include Sister Chromatid Cohesion, Chromosome Segregation, Dna Repair, Pathogenesis, Interphase. These pathways complement our catalog of research reagents for the study of Cornelia De Lange Syndrome including antibodies and ELISA kits against CCCTC-BINDING FACTOR, NOTCH, DU, CHAT, IGF2.
Top Research Reagents
We have 1627 products for the study of Cornelia De Lange Syndrome that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Cornelia De Lange Syndrome is also known as cornelia de lange syndrome, de lange syndrome, brachmann de lange syndrome, typus degenerativus amstelodamensis, de lange syndrome (disorder), des syndrome.