Chromosome painting using FISH (fluorescence in situ hybridization) with chromosome‐6‐specific library demonstrates the origin of a de novo 6q+ marker chromosome
- 1 May 1993
- journal article
- case report
- Published by Wiley in Clinical Genetics
- Vol. 43 (5) , 235-239
- https://doi.org/10.1111/j.1399-0004.1993.tb03809.x
Abstract
Brøndum‐Nielsen K, Bajalica S, Wulff K, Mikkelsen M. Chromosome painting using FISH (fluorescence in situ hybridization) with chromosome‐6‐specific library demonstrates the origin of a de novo 6q+ marker chromosome.Clin Genet 1993: 43: 235–239. © Munksgaard, 1993We report the application of chromosome painting using FISH (fluorescence in situ hybridization) to demonstrate the origin of a de novo 6q + marker chromosome. A girl with a mental retardation/multiple malformation syndrome was shown to have the karyotype 46,XX, 6q+. Banding analysis could not determine the origin of the extra chromosomal material. Using FISH with a chromosome‐6‐specific library we showed that the marker chromosome was completely painted, indicating an origin from chromosome 6. The child's phenotype was compared with previously reported cases with partial chromosome 6 trisomy. A clinically recognized syndrome emerged, although she apparently also demonstrated novel features.Keywords
This publication has 14 references indexed in Scilit:
- A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.Journal of Medical Genetics, 1992
- Reassessment of a chromosome 12q + marker by fluorescent in situ hybridization (FISH)Clinical Genetics, 1992
- Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysisHuman Genetics, 1992
- Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.Journal of Medical Genetics, 1992
- Prenatal investigation of a 45,X/46,X,r(?) karyotype in amniocytes using fluorescence in situ hybridization with an X‐centromeric probePrenatal Diagnosis, 1992
- Molecular identification of a small supernumerary marker chromosome by in situ hybridization: diagnosis of an isochromosome 18p with probe L1.84Clinical Genetics, 1991
- Genomic imprinting and the strange case of the insulin-like growth factor II receptorCell, 1991
- Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.Proceedings of the National Academy of Sciences, 1988
- Partial trisomy 6q and bilateral retinal detachmentOphthalmic Paediatrics and Genetics, 1986
- Duplication 6q24 → 6qter in an infant from a balanced paternal translocationAmerican Journal of Medical Genetics, 1983