Literature DB >> 1247018

Nonrandom distribution of exchange points in patients with structural rearrangements.

Y Nakagome, H Chiyo.   

Abstract

High resolution studies of structural rearrangements were carried out using the G-band technique. A total of 220 breakage points were identified within individual bands from 117 unrelated cases born with a structural rearrangement. Breakage points were not evenly distributed along chromosomes in terms of G-band patterns. There was an excess involvement of light bands and a striking lack of dark bands in both reciprocal translocations and inversions. In reciprocal translocations, the middle part of a chromosome arm has less chance of being the site of an exchange than the terminal and centromeric parts. The implications of these results are briefly discussed.

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Year:  1976        PMID: 1247018      PMCID: PMC1684910     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  51 in total

1.  [Familial balanced translocation t(2; 13) (q32; q33) and partial trisomy 2q].

Authors:  A Forabosco; B Dutrillaux; G Toni; G Tamborino; G Cavazzuti
Journal:  Ann Genet       Date:  1973-12

2.  Partial trisomy 8 (8q24) and the trisomy-8 syndrome.

Authors:  O Sánchez; J J Yunis
Journal:  Humangenetik       Date:  1974

3.  Different forms of incomplete trisomy 13. Mosaicism and partial trisomy for the proxim.

Authors:  A Schinzel; W Schmid
Journal:  Humangenetik       Date:  1974

4.  Identification of a large submetacentric X chromosome as pericentric inversion of an isochromosome of the long arm.

Authors:  U Ruthner; E Golob
Journal:  Humangenetik       Date:  1974-05-17

5.  Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother.

Authors:  N Hobolth; P Jacobsen; M Mikkelsen
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

6.  Precise identification of various chromosomal abnormalities.

Authors:  K Hirschhorn; M Lucas; I Wallace
Journal:  Ann Hum Genet       Date:  1973-04       Impact factor: 1.670

7.  Assignment by deletion of human red cell acid phosphatase gene locus to the short arm of chromosome 2.

Authors:  M A Ferguson-Smith; B F Newman; P M Ellis; D M Thomson; I D Riley
Journal:  Nat New Biol       Date:  1973-06-27

8.  Position of the Duffy locus on chromosome 1 in relation to breakpoints for structural rearrangements.

Authors:  C S Lee; K L Ying; P Bowen
Journal:  Am J Hum Genet       Date:  1974-01       Impact factor: 11.025

9.  Tentative localization of a Hageman (Factor XII) locus on 7q, probably the 7q35 band.

Authors:  J de Grouchy; C Turleau
Journal:  Humangenetik       Date:  1974

10.  Distribution of mitomycin C-induced damage in human chromosomes with special reference to regions of repetitive DNA.

Authors:  C A Bourgeois
Journal:  Chromosoma       Date:  1974       Impact factor: 4.316

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  9 in total

Review 1.  Arrangement of chromatin in the nucleus.

Authors:  D E Comings
Journal:  Hum Genet       Date:  1980-02       Impact factor: 4.132

2.  Nonrandom distribution of exchange points in patients with reciprocal translocations.

Authors:  C Stoll
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

3.  Hotspots of mutation and breakage in dog and human chromosomes.

Authors:  Caleb Webber; Chris P Ponting
Journal:  Genome Res       Date:  2005-12       Impact factor: 9.043

4.  Localization by Q-banding of mitotic chiasmata in cases of Bloom's syndrome.

Authors:  E M Kuhn
Journal:  Chromosoma       Date:  1976-08-04       Impact factor: 4.316

Review 5.  Pericentric inversions. Problems and significance for clinical genetics.

Authors:  P Kaiser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

Review 6.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  X-autosome translocations: cytogenetic characteristics and their consequences.

Authors:  M G Mattei; J F Mattei; S Ayme; F Giraud
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

8.  FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormality.

Authors:  J A Fantes; E Boland; J Ramsay; D Donnai; M Splitt; J A Goodship; H Stewart; M Whiteford; P Gautier; L Harewood; S Holloway; F Sharkey; E Maher; V van Heyningen; J Clayton-Smith; D R Fitzpatrick; G C M Black
Journal:  Am J Hum Genet       Date:  2008-03-27       Impact factor: 11.025

Review 9.  Distribution of break points in human structural rearrangements.

Authors:  Y Nakagome; T Matsubara; H Fujita
Journal:  Am J Hum Genet       Date:  1983-03       Impact factor: 11.025

  9 in total

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