Literature DB >> 648173

Rearrangements involving four chromosomes in a child with congenital abnormalities.

M Seabright, N Gregson, E Pacifico, S Mould, J Ryde, J Pearson, A Bradley.   

Abstract

This report describes a complex structural rearrangement between chromosomes X and 1 and a 7;13 translocation (together involving six break points) in a child with multiple congenital defects. Both parents showed a normal chromosome complement, suggesting that the changes may have originated either in a gametic nucleus or at a very early stage of zygotic development.

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Mesh：

Year:  1978        PMID： 648173     DOI： 10.1159/000130846

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


  8 in total

1.  A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences.

Authors:  Natalia Trpchevska; Ivanka Dimova; Tatyana Arabadji; Tanya Milachich; Svetlana Angelova; Magdalena Dimitrova; Mariela Hristova-Savova; Petya Andreeva; Tania Timeva; Atanas Shterev
Journal:  J Assist Reprod Genet       Date:  2017-02-24       Impact factor: 3.412

2.  Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement.

Authors:  M H Bogart; C L Bradshaw; O W Jones; J E Schanberger
Journal:  J Med Genet       Date:  1986-04       Impact factor: 6.318

3.  Familial complex autosomal translocations involving chromosomes 7, 8, and 9 exhibiting male and female transmission with segregation and recombination.

Authors:  S Walker; P J Howard; D Hunter
Journal:  J Med Genet       Date:  1985-12       Impact factor: 6.318

4.  Segregation of a complex rearrangement of chromosomes 6, 7, 8, and 12 through three generations.

Authors:  B Meer; G Wolff; E Back
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

5.  Mosaic Down's syndrome with de novo 45,XX,-21,-22,+t(21q;22q)/46,XX,-21,+t(21q;21q) rearrangement.

Authors:  A T Tharapel; R Redheendran; C B Mankinen; M K Kukolich
Journal:  J Med Genet       Date:  1984-10       Impact factor: 6.318

6.  Complex balanced translocation of chromosomes 2, 3, and 13.

Authors:  R S Muneer; D L Donaldson; O M Rennert
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  A complex double translocation involving four chromosomes and five breakpoints in a child with mild mental retardation.

Authors:  D A Couzin; J L Watt; I A Auchterlonie
Journal:  J Med Genet       Date:  1983-10       Impact factor: 6.318

8.  A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus.

Authors:  G Simoni; E Montali; F Rossella; L Dalprà; F Lo Curto
Journal:  Hum Genet       Date:  1979-01-25       Impact factor: 4.132
  8 in total

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