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Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential Alu PCR fingerprint cloning.
- Source :
-
Cytogenetics and cell genetics [Cytogenet Cell Genet] 1993; Vol. 62 (4), pp. 231-5. - Publication Year :
- 1993
-
Abstract
- Differential Alu PCR fingerprint cloning was used to isolate a DNA probe from the Xp11.4-->p11.21 region of the human X chromosome. This novel sequence, cpXr318 (DXS742), detects a new submicroscopic deletion interval at the Norrie disease locus (NDP). Combining our data with the consensus genetic map of the proximal short arm of the X chromosome, we propose the physical order Xcen-DXS14-DXS255-(DXS426, TIMP)-(DXS742-([MAOB-MAOA-DXS7], NDP)-DXS77-DXS228)-DXS209-DXS148-DXS196-++ +Xpter. The cpXr318 probe and a subclone from a cosmid corresponding to the DXS7 locus were converted into sequence-tagged sites. Finally, DXS742, DSX7, DXS77, and MAOA were integrated into a physical map spanning the Norrie disease locus.
- Subjects :
- Base Sequence
Cell Line
Chromosome Mapping
Cloning, Molecular
Genetic Markers
Humans
Hybrid Cells
Molecular Sequence Data
Polymerase Chain Reaction
Repetitive Sequences, Nucleic Acid
Restriction Mapping
Retina abnormalities
Sequence Tagged Sites
Blindness genetics
Chromosome Deletion
DNA Probes
X Chromosome
Subjects
Details
- Language :
- English
- ISSN :
- 0301-0171
- Volume :
- 62
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Cytogenetics and cell genetics
- Publication Type :
- Academic Journal
- Accession number :
- 8440142
- Full Text :
- https://doi.org/10.1159/000133484