Literature DB >> 2705455

The probability of detecting the origin of nondisjunction of autosomal trisomies.

A Chakravarti1.   

Abstract

For studying the biology of autosomal trisomies it is necessary to establish the parental origin and meiotic stage of nondisjunction by using genetic markers. Theoretical formulas are obtained for calculating the probability of establishing (1) parental origin and meiotic stage of nondisjunction by using a centromeric marker, (2) parental origin of nondisjunction by using a noncentromeric marker, and (3) meiotic stage, given parental origin of nondisjunction. These theoretical calculations demonstrate that parental origin of nondisjunction can be identified with virtual certainty by utilizing multiple genetic markers along a chromosome arm. Centromeric markers are by themselves inefficient for determining meiotic stage of the error, but the efficiency can be considerably increased if parental origin is known with certainty. Even then, multiple centromeric markers may be necessary.

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Year:  1989        PMID: 2705455      PMCID: PMC1715629     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  17 in total

1.  On the origin of the supernumerary chromosome in autosomal trisomies--with special reference to Down's syndrome. A bias in tracing nondisjunction by chromosomal and biochemical polymorphisms.

Authors:  U Langenbeck; I Hansmann; B Hinney; V Hönig
Journal:  Hum Genet       Date:  1976-07-27       Impact factor: 4.132

2.  Human chromosome heteromorphisms (variants).

Authors:  P A Jacobs
Journal:  Prog Med Genet       Date:  1977

3.  DSLINK: a computer program for gene-centromere linkage analysis in families with a trisomic offspring.

Authors:  S L Halloran; A Chakravarti
Journal:  Am J Hum Genet       Date:  1987-09       Impact factor: 11.025

4.  The use of DNA probes to establish parental origin in Down syndrome.

Authors:  N L Rudd; L S Dimnik; C Greentree; K Mendes-Crabb; D I Hoar
Journal:  Hum Genet       Date:  1988-02       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.  Cytogenetic and molecular studies of trisomy 13.

Authors:  T Hassold; P A Jacobs; M Leppert; M Sheldon
Journal:  J Med Genet       Date:  1987-12       Impact factor: 6.318

7.  Parental origin of autosomal trisomies.

Authors:  T Hassold; D Chiu; J A Yamane
Journal:  Ann Hum Genet       Date:  1984-05       Impact factor: 1.670

Review 8.  Trisomy in man.

Authors:  T J Hassold; P A Jacobs
Journal:  Annu Rev Genet       Date:  1984       Impact factor: 16.830

9.  Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndrome.

Authors:  K E Davies; K Harper; D Bonthron; R Krumlauf; A Polkey; M E Pembrey; R Williamson
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

10.  Methods for studying recombination on chromosomes that undergo nondisjunction.

Authors:  A Chakravarti; S A Slaugenhaupt
Journal:  Genomics       Date:  1987-09       Impact factor: 5.736

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  7 in total

1.  Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.

Authors:  M B Peterson; M Frantzen; S E Antonarakis; A C Warren; C Van Broeckhoven; A Chakravarti; T K Cox; C Lund; B Olsen; H Poulsen
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

2.  dNORs and meiotic nondisjunction.

Authors:  S Schwartz; D Roulston; M M Cohen
Journal:  Am J Hum Genet       Date:  1989-05       Impact factor: 11.025

3.  A molecular genetic approach to the identification of isochromosomes of chromosome 21.

Authors:  L G Shaffer; C K Jackson-Cook; J M Meyer; J A Brown; J E Spence
Journal:  Hum Genet       Date:  1991-02       Impact factor: 4.132

4.  Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome.

Authors:  M B Petersen; A A Schinzel; F Binkert; L Tranebjaerg; M Mikkelsen; F A Collins; E P Economou; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

5.  Parental origin of the extra chromosome in trisomy 18.

Authors:  K G Kupke; U Müller
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

Review 6.  Detection of cryptic chromosomal abnormalities in unexplained mental retardation: a general strategy using hypervariable subtelomeric DNA polymorphisms.

Authors:  A O Wilkie
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

7.  Discerning non-disjunction in Down syndrome patients by means of GluK1-(AGAT)(n) and D21S2055-(GATA)(n) microsatellites on chromosome 21.

Authors:  Debarati Ghosh; Swagata Sinha; Anindita Chatterjee; Krishnadas Nandagopal
Journal:  Indian J Hum Genet       Date:  2012-05
  7 in total

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