ArticleHuman genetics1993
The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting.
Article in Human genetics, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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13 citing papers in PubMed, 50 citations in OpenAlex.
- De Novo Subtelomeric 6p25.3 Deletion with Duplication of 6q23.3-q27: Genotype-Phenotype Correlation.Journal of pediatric genetics · 2020Article
- Molecular characterization of a de novo 6q24.2q25.3 duplication interrupting UTRN in a patient with arthrogryposis.American journal of medical genetics. Part A · 2010Article
- Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisation.Journal of medical genetics · 1998Article
- Characterization of marker chromosomes by fish using microdissected probes from old Carnoy-fixed cells: report of two cases.The Japanese journal of human genetics · 1997Article
- Fish mapping of a translocation breakpoint at 6q21 (or q22) in a patient with heterotaxia.The Japanese journal of human genetics · 1997Article
- Rapid identification of multiple supernumerary ring chromosomes with a new FISH technique.Journal of medical genetics · 1997Article
- Assignment of the human connexin43 gene, GJA1, to chromosome 6q22.3.The Japanese journal of human genetics · 1997Article
- Familial complex chromosome rearrangement ascertained by in situ hybridisation.Journal of medical genetics · 1997Article
- A 3 1/2 year old girl with distal trisomy 19q defined by FISH.Journal of medical genetics · 1996Article
- Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISH.Journal of medical genetics · 1996Article
- Complete and precise characterization of marker chromosomes by application of microdissection in prenatal diagnosis.Human genetics · 1995Article
- Identification of the origin of double minutes in normal human cells by laser-based chromosome microdissection approach.Human genetics · 1995Article
- A stable acentric marker chromosome: possible existence of an intercalary ancient centromere at distal 8p.American journal of human genetics · 1994Article
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Authors and funding
8 authors at 4 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
De novo chromosome structural abnormalities cannot always be diagnosed by the use of standard cytogenetic techniques. We applied a previously developed chromosome-band-specific painting method to the diagnosis of such rearrangements. The diagnostic procedures consisted of microdissection of an aberrant chromosomal region of a given patient, polymerase chain reaction (PCR) amplification of the dissected chromosomal DNA, and subsequent competitive fluorescence in situ hybridization (FISH) using the PCR products as a probe pool on metaphase chromosomes from the patient and/or a karyotypically normal person. With this strategy, we studied 6 de novo rearrangements (6p+, 6q+, 9p+, 17p+, +mar, and +mar) in 6 patients. These rearrangements had been seen by conventional banding but their origin could not be identified. In all 6 patients, we successfully ascertained the origin. Using an aberrant region-specific probe pool, FISH signals appeared on both the aberrant region and a region of another specific chromosome pair. A reverse probe pool that was generated through the microdissection of normal chromosomes at a candidate region for the origin of the aberration hybridized with both the aberrant and the candidate regions. We thus diagnosed one patient with 17p+ as having trisomy for 14q32-qter, one with 9p+ as having trisomy for 12pter-p12, one with 6q+ as having a tandem duplication (trisomy) of a 6q23-q25 segment, one with 6p+ as having a tandem duplication (trisomy) of a 6p23-q21.3 segment, one with a supernumerary metacentric marker chromosome as having tetrasomy for 18pter-cen, and the last with an additional small marker chromosome as having trisomy for 18p11.1 (or p11.2)-q11.2. The present targeted chromosome-band-painting method provides the simple and rapid preparation of a probe pool for region-specific FISH, and is useful for the diagnosis of chromosome abnormalities of unknown origin.
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