Pages that link to "Q33627578"
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The following pages link to Altered intra-nuclear organisation of heterochromatin and genes in ICF syndrome (Q33627578):
Displaying 13 items.
- Spatial Genome Organization and Its Emerging Role as a Potential Diagnosis Tool (Q26738275) (← links)
- Dnmt3b Prefers Germ Line Genes and Centromeric Regions: Lessons from the ICF Syndrome and Cancer and Implications for Diseases (Q27009992) (← links)
- Germline genes hypomethylation and expression define a molecular signature in peripheral blood of ICF patients: implications for diagnosis and etiology (Q33615784) (← links)
- The role of genetics in the establishment and maintenance of the epigenome. (Q34649133) (← links)
- Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2. (Q35040223) (← links)
- Role of DNMT3B in the regulation of early neural and neural crest specifiers (Q35897290) (← links)
- Role of Nuclear Architecture in Epigenetic Alterations in Cancer (Q36155532) (← links)
- Constitutional Epi/Genetic Conditions: Genetic, Epigenetic, and Environmental Factors (Q39127494) (← links)
- Scanning electron microscope studies of human metaphase chromosomes (Q41887587) (← links)
- A novel deletion in ZBTB24 in a Lebanese family with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2. (Q43449433) (← links)
- 3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome (Q84068033) (← links)
- Chromosome variant 1qh- and its influence on the 3D organization of chromosome 1 heterochromatin in interphase nucleus of patients with endometriosis (Q87905133) (← links)
- Keeping the Centromere under Control: A Promising Role for DNA Methylation (Q92702684) (← links)