Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Chromosome in situ suppression hybridisation in clinical cytogenetics.

Literature DB >> 1956055

Chromosome in situ suppression hybridisation in clinical cytogenetics.

M A Hulten¹, C P Gould, A S Goldman, J J Waters.

Abstract

The use of chromosome in situ suppression hybridisation with whole chromosome libraries has previously been reported by various research laboratories to be an effective method of identifying specific human chromosomal material. As a clinical cytogenetic service laboratory we have used the technique as a complement to diagnosis by classical chromosome banding. In three examples of structural rearrangements the potential use of the 'chromosome painting' method is assessed for its ability to enhance the routine cytogenetic service currently available.

Entities: Species

Mesh：

Year: 1991 PMID： 1956055 PMCID： PMC1015785 DOI： 10.1136/jmg.28.9.577

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

7 in total

1. Detection of the Philadelphia chromosome in interphase nuclei.

Authors: E P Arnoldus; J Wiegant; I A Noordermeer; J W Wessels; G C Beverstock; G C Grosveld; M van der Ploeg; A K Raap
Journal: Cytogenet Cell Genet Date: 1990

2. Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics.

Authors: A Jauch; C Daumer; P Lichter; J Murken; T Schroeder-Kurth; T Cremer
Journal: Hum Genet Date: 1990-07 Impact factor: 4.132

3. Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries.

Authors: P Lichter; T Cremer; J Borden; L Manuelidis; D C Ward
Journal: Hum Genet Date: 1988-11 Impact factor: 4.132

4. Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes.

Authors: T Cremer; P Lichter; J Borden; D C Ward; L Manuelidis
Journal: Hum Genet Date: 1988-11 Impact factor: 4.132

5. Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

Authors: D Pinkel; J Landegent; C Collins; J Fuscoe; R Segraves; J Lucas; J Gray
Journal: Proc Natl Acad Sci U S A Date: 1988-12 Impact factor: 11.205

6. Rapid detection of human chromosome 21 aberrations by in situ hybridization.

Authors: P Lichter; T Cremer; C J Tang; P C Watkins; L Manuelidis; D C Ward
Journal: Proc Natl Acad Sci U S A Date: 1988-12 Impact factor: 11.205

7. The Marfan syndrome locus: confirmation of assignment to chromosome 15 and identification of tightly linked markers at 15q15-q21.3.

Authors: H C Dietz; R E Pyeritz; B D Hall; R G Cadle; A Hamosh; J Schwartz; D A Meyers; C A Francomano
Journal: Genomics Date: 1991-02 Impact factor: 5.736

7 in total

6 in total

1. Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.

Authors: N P Carter; M A Ferguson-Smith; M T Perryman; H Telenius; A H Pelmear; M A Leversha; M T Glancy; S L Wood; K Cook; H M Dyson
Journal: J Med Genet Date: 1992-05 Impact factor: 6.318

Review 2. Demystified ... FISH.

Authors: J J Waters; A L Barlow; C P Gould
Journal: Mol Pathol Date: 1998-04

6. Germinal and Somatic Trisomy 21 Mosaicism: How Common is it, What are the Implications for Individual Carriers and How Does it Come About?

Authors: Maj A Hultén; Jon Jonasson; Ann Nordgren; Erik Iwarsson
Journal: Curr Genomics Date: 2010-09 Impact factor: 2.236