Physical map of human Xq27-qter: Localizing the region of the fragile X mutation
Journal Article
·
· Proceedings of the National Academy of Sciences of the United States of America; (United States)
- Deutsches Krebsforschungszentrum, Heidelberg (West Germany)
- Istituto di Genetica Biochemica ed Evoluzionistica, Pavia (Italy)
- Emory Univ., Atlanta, GA (United States)
- Imperial Cancer Research Fund, London (England)
The authors describe a physical map of the end of the long arm of the human X chromosome encompassing the region from Xq27.2 to the q telomere, inclusive of the chromosomal band Xq28. This region is of particular interest, since it contains the highest density of genes associated with genetic diseases. The map covers a total of 12 megabases (Mb) of DNA and extends from the telomere to 3 Mb beyond the most likely position of the fragile X mutation, defined by a cluster of translocation breakpoints in somatic cell hybrids. The map determines order and position of loci throughout the Xq28 region and localizes cell line breakpoints marking the fragile X region to an interval of 300-700 kilobases between 8 and 8.7. Mb proximal of the Xq telomere.
- OSTI ID:
- 5821640
- Journal Information:
- Proceedings of the National Academy of Sciences of the United States of America; (United States), Journal Name: Proceedings of the National Academy of Sciences of the United States of America; (United States) Vol. 88:19; ISSN 0027-8424; ISSN PNASA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
550400* -- Genetics
59 BASIC BIOLOGICAL SCIENCES
AZINES
CHROMOSOMES
DISEASES
DNA HYBRIDIZATION
ELECTROPHORESIS
GENE MUTATIONS
GENETIC MAPPING
HEREDITARY DISEASES
HETEROCHROMOSOMES
HETEROCYCLIC COMPOUNDS
HUMAN CHROMOSOMES
HUMAN X CHROMOSOME
HYBRIDIZATION
MAPPING
MUTATIONS
NUCLEOSIDES
NUCLEOTIDES
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
PYRIMIDINES
RIBOSIDES
THYMIDINE
X CHROMOSOME
59 BASIC BIOLOGICAL SCIENCES
AZINES
CHROMOSOMES
DISEASES
DNA HYBRIDIZATION
ELECTROPHORESIS
GENE MUTATIONS
GENETIC MAPPING
HEREDITARY DISEASES
HETEROCHROMOSOMES
HETEROCYCLIC COMPOUNDS
HUMAN CHROMOSOMES
HUMAN X CHROMOSOME
HYBRIDIZATION
MAPPING
MUTATIONS
NUCLEOSIDES
NUCLEOTIDES
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
PYRIMIDINES
RIBOSIDES
THYMIDINE
X CHROMOSOME