Literature DB >> 2316522

The parental origin of the extra X chromosome in 47,XXX females.

K M May1, P A Jacobs, M Lee, S Ratcliffe, A Robinson, J Nielsen, T J Hassold.   

Abstract

We used X-linked DNA polymorphisms to study the parental origin of X chromosome nondisjunction in 28 47,XXX live-born females. Errors in oogenesis accounted for 26 of the cases, with the majority of these being attributable to an error at meiosis I. We observed an association between advanced parental age and meiosis I nondisjunction--but not meiosis II nondisjunction--in the maternally derived cases. In studies of recombination we found little evidence for an association between pairing failure and X chromosome nondisjunction, but our results suggest that increased recombination near the centromere may play a role in the etiology of the 47,XXX condition.

Mesh：

Year:  1990        PMID： 2316522      PMCID： PMC1683670     

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


  20 in total

1.  Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes.

Authors:  P A Jacobs; T J Hassold; E Whittington; G Butler; S Collyer; M Keston; M Lee
Journal:  Ann Hum Genet       Date:  1988-05       Impact factor: 1.670

2.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

Authors:  P W Rigby; M Dieckmann; C Rhodes; P Berg
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

3.  Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22.

Authors:  N J Fraser; Y Boyd; I Craig
Journal:  Genomics       Date:  1989-07       Impact factor: 5.736

4.  A simple salting out procedure for extracting DNA from human nucleated cells.

Authors:  S A Miller; D D Dykes; H F Polesky
Journal:  Nucleic Acids Res       Date:  1988-02-11       Impact factor: 16.971

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.  Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.

Authors:  K K Kidd; A M Bowcock; J Schmidtke; R K Track; F Ricciuti; G Hutchings; A Bale; P Pearson; H F Willard; J Gelernter
Journal:  Cytogenet Cell Genet       Date:  1989

7.  Xg groups and sex abnormalities in people of northern European ancestry.

Authors:  R Sanger; P Tippett; J Gavin
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

8.  Cytogenetic and molecular analysis of sex-chromosome monosomy.

Authors:  T Hassold; F Benham; M Leppert
Journal:  Am J Hum Genet       Date:  1988-04       Impact factor: 11.025

9.  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

10.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1983-07-01       Impact factor: 3.365
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  25 in total

1.  Autism in association with Triple X syndrome.

Authors:  Syed Irfan Ali; Nollaig Byrne; Aisling Mulligan
Journal:  Eur Child Adolesc Psychiatry       Date:  2012-02-04       Impact factor: 4.785

2.  Scrambling eggs: meiotic drive and the evolution of female recombination rates.

Authors:  Yaniv Brandvain; Graham Coop
Journal:  Genetics       Date:  2011-12-05       Impact factor: 4.562

Review 3.  Meiotic origins of maternal age-related aneuploidy.

Authors:  Teresa Chiang; Richard M Schultz; Michael A Lampson
Journal:  Biol Reprod       Date:  2012-01-10       Impact factor: 4.285

4.  The parental origin of the single X chromosome in Turner syndrome: lack of correlation with parental age or clinical phenotype.

Authors:  A Mathur; L Stekol; D Schatz; N K MacLaren; M L Scott; B Lippe
Journal:  Am J Hum Genet       Date:  1991-04       Impact factor: 11.025

5.  A cytogenetic and molecular study of a series of 45,X fetuses and their parents.

Authors:  A Cockwell; M MacKenzie; S Youings; P Jacobs
Journal:  J Med Genet       Date:  1991-03       Impact factor: 6.318

6.  Parental origin and mechanism of formation of polysomy X: an XXXXX case and four XXXXY cases determined with RFLPs.

Authors:  H X Deng; K Abe; I Kondo; M Tsukahara; H Inagaki; I Hamada; Y Fukushima; N Niikawa
Journal:  Hum Genet       Date:  1991-04       Impact factor: 4.132

7.  Association between nondisjunction and maternal age in meiosis-II human oocytes.

Authors:  T Dailey; B Dale; J Cohen; S Munné
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

8.  XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region.

Authors:  T J Hassold; S L Sherman; D Pettay; D C Page; P A Jacobs
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

9.  Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy.

Authors:  T Hassold; D Pettay; K May; A Robinson
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

Review 10.  New Solutions to Old Problems: Molecular Mechanisms of Meiotic Crossover Control.

Authors:  Gerald R Smith; Mridula Nambiar
Journal:  Trends Genet       Date:  2020-03-21       Impact factor: 11.639
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