3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome. [electronic resource]
Producer: 20121113Description: 187-92 p. digitalISSN:- 1399-0004
- Adolescent
- Cell Nucleus -- genetics
- Centromere
- Chromosome Aberrations
- Chromosomes, Human, Pair 1
- Chromosomes, Human, Pair 9
- DNA Methylation
- DNA, Satellite
- Face -- abnormalities
- Female
- Heterochromatin -- chemistry
- Humans
- Immunologic Deficiency Syndromes -- diagnosis
- In Situ Hybridization, Fluorescence
- Primary Immunodeficiency Diseases
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Publication Type: Case Reports; Journal Article
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