Literature DB >> 8880585

Diagnosis of a complex chromosomal rearrangement using fluorescent in situ hybridisation.

R Wallerstein1, L Gibas, C E Anderson, L Jackson.   

Abstract

We report the use of fluorescent in situ hybridisation (FISH) to clarify a complex chromosomal rearrangement (CCR) carried by a woman presenting with recurrent miscarriages. CCRs are rare cytogenetic rearrangements involving three or more chromosomes, which can be difficult to interpret using routine cytogenetic studies with GTG banding. FISH was used to establish a correct interpretation of the maternal karyotype before amniocentesis in a present pregnancy.

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Year:  1996        PMID： 8880585      PMCID： PMC1050739          DOI： 10.1136/jmg.33.9.793

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


  8 in total

1.  Analysis of reciprocal translocations by chromosome painting: applications and limitations of the technique.

Authors:  C Rosenberg; K J Blakemore; W G Kearns; R A Giraldez; C S Escallon; P L Pearson; G Stetten
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

2.  Reproductive risks for carriers of complex chromosome rearrangements: analysis of 25 families.

Authors:  J L Gorski; M L Kistenmacher; H H Punnett; E H Zackai; B S Emanuel
Journal:  Am J Med Genet       Date:  1988-02

Review 3.  Complex chromosomal rearrangement in a woman with multiple miscarriages.

Authors:  K Kausch; T Haaf; J Köhler; M Schmid
Journal:  Am J Med Genet       Date:  1988-10

4.  Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis.

Authors:  H Wang; M McLaughlin; C Thompson; A G Hunter
Journal:  Am J Med Genet       Date:  1993-06-15

Review 5.  Complex chromosomal rearrangements (CCR) and their genetic consequences.

Authors:  A Kleczkowska; J P Fryns; H Van den Berghe
Journal:  J Genet Hum       Date:  1982-10

6.  A complex three breakpoint translocation involving chromosomes 2, 4, and 9 identified by meiotic investigations of a human male ascertained for subfertility.

Authors:  N Saadallah; M Hulten
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

Review 7.  The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features.

Authors:  E Niebuhr
Journal:  Hum Genet       Date:  1978-11-16       Impact factor: 4.132

Review 8.  Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.

Authors:  D A Batista; G S Pai; G Stetten
Journal:  Am J Med Genet       Date:  1994-11-15
  8 in total
  1 in total

1.  A new approach to the elucidation of complex chromosome rearrangements illustrated by a case of Rieger syndrome.

Authors:  C M Ogilvie; F L Raymond; R H Harrison; P N Scriven; Z Docherty
Journal:  J Med Genet       Date:  1998-03       Impact factor: 6.318
  1 in total

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