Literature DB >> 148352

The origin of the extra chromosome 21 in Down syndrome. Studies of fluorescent variants and satelite association in 26 informative families.

A Hansson, M Mikkelsen.   

Abstract

Studies of fluorescence and other chromosomal variants were informative in 26 out of 72 families. Maternal nondisjunction was found in 19 and paternal in 7 cases. Satellite association studies of these parents and 94 controls from the same age group showed a highly significant increase in the satellite association index (AI) for chromosome 21 in the parents where the nondisjunctional event had taken place. The AI was also higher for chromosome 14. In addition, the parents who produced the normal gametes had significantly higher AI's for some acrocentrics than the controls. Exogenous factors increasing satellite association cannot be ruled out. The number of 21-21 association was significantly increased in the parents with nondisjunction in meiosis 1. The results indicate that satellite association may play a role in the etiology of Down syndrome.

Mesh:

Year:  1978        PMID: 148352     DOI: 10.1159/000130851

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


  18 in total

1.  Paternal age and trisomy among spontaneous abortions.

Authors:  M Hatch; J Kline; B Levin; M Hutzler; D Warburton
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132

2.  Nucleolar organizer region variants as a risk factor for Down syndrome.

Authors:  C K Jackson-Cook; D B Flannery; L A Corey; W E Nance; J A Brown
Journal:  Am J Hum Genet       Date:  1985-11       Impact factor: 11.025

3.  De novo 21/21 translocation Down syndrome. Studies of parental origin of the translocation and acrocentric associations in parents.

Authors:  J Nikolis; V Kekić
Journal:  Hum Genet       Date:  1986-06       Impact factor: 4.132

4.  Comparison of acrocentric associations in male and female cells. Relationship to the active nucleolar organizers.

Authors:  H Galperin-Lemaître; L Hens; B Sele
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

5.  Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.

Authors:  G D Stewart; T J Hassold; A Berg; P Watkins; R Tanzi; D M Kurnit
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

6.  Reexamination of paternal age effect in Down's syndrome.

Authors:  M P Roth; J Feingold; A Baumgarten; P Bigel; C Stoll
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

7.  Paternal age and Down's syndrome genotypes diagnosed prenatally: no association in New York state data.

Authors:  E B Hook; P K Cross
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

8.  Paternal age and Down syndrome in British Columbia.

Authors:  E B Hook; P K Cross; S H Lamson; R R Regal; P A Baird; S H Uh
Journal:  Am J Hum Genet       Date:  1981-01       Impact factor: 11.025

9.  Chromosomal abnormalities in human sperm: comparisons among four healthy men.

Authors:  B Brandriff; L Gordon; L Ashworth; G Watchmaker; A Carrano; A Wyrobek
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

Review 10.  Molecular genetics of human chromosome 21.

Authors:  P C Watkins; R E Tanzi; S V Cheng; J F Gusella
Journal:  J Med Genet       Date:  1987-05       Impact factor: 6.318

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