Literature DB >> 138745

A fluorescence polymorphism associated with Down's syndrome?

J A Robinson, M Newton.   

Abstract

Fluorescence polymorphism frequencies have been determined for a group of 85 Down's syndrome cases and 164 controls. For one class of polymorphism, that of positive satellites of chromosome 21, the frequency in the Down's cases was significantly higher than in the controls; the distribution of positive satellites in the mongols indicates that in the majority the extra chromosome arose by first meiotic non-disjunction. The possibility that positive satellites on chromosome 21 could be a causative factor in Down's syndrome is discussed, and the implications of this possibility on the assessment of the risk of producing a Down's child are examined.

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Year:  1977        PMID: 138745      PMCID: PMC1013505          DOI: 10.1136/jmg.14.1.40

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  5 in total

1.  Origin of the trisomic 21 chromosome.

Authors:  D E Mutton
Journal:  Lancet       Date:  1973-02-17       Impact factor: 79.321

2.  Origin of extra chromosome in trisomy 21.

Authors:  J A Robinson
Journal:  Lancet       Date:  1973-01-20       Impact factor: 79.321

3.  Trisomy 21 in man due to maternal non-disjunction during the first meiotic division.

Authors:  G Licznerski; J Lindsten
Journal:  Hereditas       Date:  1972       Impact factor: 3.271

4.  Leukocytes cultured from small inocula of whole blood and the preparation of metaphase chromosomes by treatment with hypotonic KCl.

Authors:  D A Hungerford
Journal:  Stain Technol       Date:  1965-11

5.  C- and Q-band polymorphisms in the chromosomes of three human populations.

Authors:  K E Buckton; M L O'Riordan; P A Jacobs; J A Robinson; R Hill; H J Evans
Journal:  Ann Hum Genet       Date:  1976-07       Impact factor: 1.670

  5 in total
  2 in total

1.  The exercise redox paradigm in the Down's syndrome: improvements in motor function and increases in blood oxidative status in young adults.

Authors:  Aderbal S Aguiar; Talita Tuon; Mirella M Albuquerque; Gláucia S Rocha; Ana E Speck; Júlio C Araújo; Alcir L Dafré; Rui D S Prediger; Ricardo A Pinho
Journal:  J Neural Transm (Vienna)       Date:  2008-09-16       Impact factor: 3.575

2.  Meiosis I non-disjunction as the main cause of trisomy 21.

Authors:  J A Robinson
Journal:  Hum Genet       Date:  1977-11-02       Impact factor: 4.132

  2 in total

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