Literature DB >> 6478637

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

F Hecht, B K Hecht.   

Abstract

Certain fragile sites may possibly predispose to chromosome breakage and rearrangements in meiosis. To test this hypothesis, we examined 894 breakpoints found in spontaneous abortions, stillbirths and livebirths of which 165 (18.5%) were in bands with fragile sites. Compared to an expectation of 98 (11%), there was a significant excess of breakpoints in fragile site bands (P less than 0.001). Together with data from amniocenteses, there is now evidence suggesting that certain fragile sites may be prone to fragility in meiosis.

Mesh:

Year:  1984        PMID: 6478637     DOI: 10.1111/j.1399-0004.1984.tb04364.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  10 in total

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

Authors:  C Fuster; R Miró; C Templado; L Barrios; V Moreno; J Egozcue
Journal:  Hum Genet       Date:  1989-07       Impact factor: 4.132

2.  Chromosome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23.

Authors:  L E Voullaire; G C Webb; M A Leversha
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

3.  Inversion of chromosome 2 (p11p13): frequency and implications for genetic counselling.

Authors:  I M MacDonald; D M Cox
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

4.  Population cytogenetics of folate-sensitive fragile sites. I. Common fragile sites.

Authors:  M Kähkönen
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

Review 5.  Genome organization and species formation in vertebrates.

Authors:  G Bernardi
Journal:  J Mol Evol       Date:  1993-10       Impact factor: 2.395

6.  Multicolor FISH analysis of chromosomal breaks, duplications, deletions, and numerical abnormalities in the sperm of healthy men.

Authors:  E D Sloter; X Lowe; D H Moore II; J Nath; A J Wyrobek
Journal:  Am J Hum Genet       Date:  2000-08-28       Impact factor: 11.025

7.  The significance of pericentric inversions of chromosome 2.

Authors:  M Djalali; P Steinbach; J Bullerdiek; M Holmes-Siedle; M R Verschraegen-Spae; A Smith
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

8.  Muscular dystrophy in girls with X;autosome translocations.

Authors:  Y Boyd; V Buckle; S Holt; E Munro; D Hunter; I Craig
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

9.  Pericentric inversions in man: personal experience and review of the literature.

Authors:  A Kleczkowska; J P Fryns; H Van den Berghe
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132

10.  Non-Random Distribution of Reciprocal Translocation Breakpoints in the Pig Genome.

Authors:  Brendan Donaldson; Daniel A F Villagomez; Tamas Revay; Samira Rezaei; W Allan King
Journal:  Genes (Basel)       Date:  2019-09-30       Impact factor: 4.096

  10 in total

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