Literature DB >> 2737665

Fragile sites and breakpoints in constitutional rearrangements and in human sperm chromosomes.

C Fuster1, R Miró, C Templado, L Barrios, V Moreno, J Egozcue.   

Abstract

Recently, it has been suggested that an association exists between breakpoints involved in constitutional rearrangements and fragile sites; however, statistical analyses of this relationship are controversial. We have analyzed 1200 breakpoint from different constitutional rearrangements, 1522 breakpoints with respect to their recurrence and 217 breakpoints from sperm chromosomes as reported by several authors. The coincidence between breakpoints and fragile sites was 35.3%, 43.6% and 41.9% respectively. The statistical significance of these coincidences depends on whether factors such as the relative length of the bands or the recurrence of the rearrangements are taken into account.

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Year:  1989        PMID: 2737665     DOI: 10.1007/bf00273992

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  25 in total

1.  Report of the committee on cytogenetic markers.

Authors:  G R Sutherland; J F Mattei
Journal:  Cytogenet Cell Genet       Date:  1987

Review 2.  Pericentric inversions in man. A French collaborative study. Groupe de Cytogénéticiens Français.

Authors: 
Journal:  Ann Genet       Date:  1986

3.  Fragile sites and chromosome breakpoints in constitutional rearrangements II. Spontaneous abortions, stillbirths and newborns.

Authors:  F Hecht; B K Hecht
Journal:  Clin Genet       Date:  1984-09       Impact factor: 4.438

4.  [Non random position of metaphasic chromosomes. III. Position of chromosomes involved in constitutional translocations].

Authors:  J L Antoine; A Aurias; B Dutrillaux
Journal:  Ann Genet       Date:  1982

5.  Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing.

Authors:  P Jalbert; B Sele; H Jalbert
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

6.  The 11q;22q translocation: a European collaborative analysis of 43 cases.

Authors:  M Fraccaro; J Lindsten; C E Ford; L Iselius
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

7.  Chromosome studies in 2136 couples with spontaneous abortions.

Authors:  G Bourrouillou; P Colombies; N Dastugue
Journal:  Hum Genet       Date:  1986-12       Impact factor: 4.132

8.  Paracentric inversions in man.

Authors:  J P Fryns; A Kleczkowska; H Van den Berghe
Journal:  Hum Genet       Date:  1986-07       Impact factor: 4.132

9.  Reproductive risks for translocation carriers: cytogenetic study and analysis of pregnancy outcome in 58 families.

Authors:  G Neri; A Serra; M Campana; B Tedeschi
Journal:  Am J Med Genet       Date:  1983-12

10.  Chromosomes of human sperm: variability among normal individuals.

Authors:  B Brandriff; L Gordon; L Ashworth; G Watchmaker; D Moore; A J Wyrobek; A V Carrano
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

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