Literature DB >> 2940437

A possible cause of non-disjunction of additional chromosome 21 in Down syndrome.

R S Verma, A Babu, S Chemitiganti, H Dosik.   

Abstract

A possible cause of non-disjunction of chromosome 21 in Down Syndromes has been cytogenetically evaluated by examining the parents by Ag-staining technique. In all the cases studied so far, the contributing parents have active ribosomal cistrons on both chromosomes 21 i.e. both chromosomes are stained positively by silver staining. These results show that the active NORs might play an essential role in meiotic non-disjunction. Furthermore, the preliminary results demonstrate that the acrocentric associations of homologous and non-homologous nature involving chromosome 21 are the most frequent in the contributing parent which may further indicate the role of multiple cellular factors affecting the associations in promoting the nondisjunction in addition to active NORs. The possible mechanisms regarding the non-disjunction of chromosome 21 have been described.

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Year:  1986        PMID: 2940437     DOI: 10.1007/bf00333259

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  15 in total

1.  Genetic counseling for the older pregnant woman: new data and questions.

Authors:  L B Holmes
Journal:  N Engl J Med       Date:  1978-06-22       Impact factor: 91.245

Review 2.  Structural and functional aspects of nucleolar organizer regions (NORs) of human chromosomes.

Authors:  K A Babu; R S Verma
Journal:  Int Rev Cytol       Date:  1985

3.  Demonstration of color and size polymorphisms in human acrocentric chromosomes by acridine orange reverse banding.

Authors:  R S Verma; H Dosik; H A Lubs
Journal:  J Hered       Date:  1977 Jul-Aug       Impact factor: 2.645

Review 4.  Human chromosomal heteromorphisms: nature and clinical significance.

Authors:  R S Verma; H Dosik
Journal:  Int Rev Cytol       Date:  1980

5.  Preferential association of nucleolar organizing human chromosomes as revealed by silver staining technique at mitosis.

Authors:  R S Verma; J Rodríguez; J V Shah; H Dosik
Journal:  Mol Gen Genet       Date:  1983

6.  Frequencies of chromosome and chromatid types of associations of nucleolar human chromosomes demonstrated by the N-banding technique.

Authors:  R S Verma; J V Shah; H Dosik
Journal:  Cytobios       Date:  1983

7.  Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons.

Authors:  R C Juberg; P N Mowrey
Journal:  Am J Med Genet       Date:  1983-09

8.  Evidence for genetic control of nondisjunction in man.

Authors:  O S Alfi; R Chang; S P Azen
Journal:  Am J Hum Genet       Date:  1980-07       Impact factor: 11.025

9.  A simple R banding technic.

Authors:  R S Verma; H A Lubs
Journal:  Am J Hum Genet       Date:  1975-01       Impact factor: 11.025

10.  Variation in human acrocentric chromosomes with acridine orange reverse banding.

Authors:  R S Verma; H A Lubs
Journal:  Humangenetik       Date:  1975-09-20
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  3 in total

1.  AluI-resistant chromatin of chromosome 18: classification, frequencies and implications.

Authors:  A Babu; R S Verma; S R Patil
Journal:  Chromosoma       Date:  1987       Impact factor: 4.316

2.  Nucleolar structures in chromosome and SC preparations from human oocytes at first meiotic prophase.

Authors:  M García; A Dietrich; R Pujol; J Egozcue
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

Review 3.  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

  3 in total

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