Literature DB >> 8322821

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

H Wang1, M McLaughlin, C Thompson, A G Hunter.   

Abstract

A balanced complex chromosome rearrangement (BCCR) involving 3 chromosomes with 4 breakpoints, was identified in a 36-yr-old woman who was studied because her fetus was discovered to have an unbalanced reciprocal translocation (7q;10q). Analysis of high resolution bands and the application of fluorescence in situ hybridization has identified the BCCR as der(7)t(7;10)(q21.13;q23.33)ins(21;7)(q21.3;q11.22q21.13), der(10)t(7;10)(q21.13; q23.33), der(21)ins(21;7)(q21.3;q11.22q21.13). Alternate segregation of the BCCR appears to be favoured, and has resulted in two pregnancies with an unbalanced chromosome constitution.

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Year:  1993        PMID: 8322821     DOI: 10.1002/ajmg.1320460520

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  4 in total

1.  Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.

Authors:  D Wieczorek; H Engels; R Viersbach; B Henke; G Schwanitz; E Passarge
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318

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

Authors:  R Wallerstein; L Gibas; C E Anderson; L Jackson
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

3.  Familial four breakpoint complex chromosomal rearrangement as a cause of monosomy 9p22-->pter and trisomy 10p11.2-->pter and 11q21 analysed by dual and triple colour FISH.

Authors:  P Stankiewicz; E Kostyk; E Bocian; H Stańczak; J Parczewska; E Piatkowska; T Mazurczak; J J Pietrzyk
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

4.  A familial "balanced" 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings.

Authors:  J Wagstaff; M Hemann
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

  4 in total

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