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High frequencies of ICF syndrome-like pericentromeric heterochromatin decondensation and breakage in chromosome 1 in a chorionic villus sample.
- Source :
-
Journal of medical genetics [J Med Genet] 2001 Dec; Vol. 38 (12), pp. 882-4. - Publication Year :
- 2001
- Subjects :
- Adult
Cells, Cultured
Centromere genetics
Chromosomes, Human, Pair 1 metabolism
Chromosomes, Human, Pair 13 genetics
Chromosomes, Human, Pair 16 genetics
Craniofacial Abnormalities metabolism
DNA (Cytosine-5-)-Methyltransferases genetics
DNA (Cytosine-5-)-Methyltransferases metabolism
DNA Methylation
Female
Gene Frequency genetics
Genetic Counseling
Genetic Testing
Heterochromatin genetics
Humans
Immunologic Deficiency Syndromes metabolism
Infant
Infant, Newborn
Male
Pregnancy
Prenatal Diagnosis
Syndrome
Trisomy genetics
DNA Methyltransferase 3B
Centromere metabolism
Chorionic Villi metabolism
Chromosome Breakage genetics
Chromosomes, Human, Pair 1 genetics
Craniofacial Abnormalities genetics
Heterochromatin metabolism
Immunologic Deficiency Syndromes genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1468-6244
- Volume :
- 38
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Journal of medical genetics
- Publication Type :
- Report
- Accession number :
- 11768395
- Full Text :
- https://doi.org/10.1136/jmg.38.12.882