Literature DB >> 511145

Structural differences in reciprocal translocations. Potential for a model of risk in Rcp.

A Daniel.   

Abstract

Interchange segment sizes and the sizes of chromosome imbalance arising from the different modes of meiotic segregation were measured in a selected sample of 20 reciprocal translocations (Rep). The Rep were selected by two modes of ascertainment: (I) neonates with an unbalanced form of the translocation, and (II) couples with recurrent spontaneous abortions without evidence of full-term translocation aneuploid offspring. The measurements (% of haploid autosomal length: %HAL) were plotted as the observed or potential chromosomal imbalance with monosomy (abscissa) and trisomy (ordinate). It was found that (a) the interchange segments were larger in the spontaneous abortion Rcp, (b) that all of the imbalances observed in full-term neonates plotted close to the origin and to the left of the line joining 4% trisomy to 2% monosomy, and (c) the imbalances observed in the neonates in each individual Rcp were of the smallest size possible arising by any segregation mode. It was concluded that a major factor in the survival to term of aneuploid conceptuses is the size (proportion of genome) of the chromosome abnormality, irrespective of the origin of the chromosome regions. These results are discussed in relation to their use as a model to evaluate the risk of abnormal offspring in the progeny of translocation heterozygotes (the Chromosome Imbalance Size-Viability Model).

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Year:  1979        PMID: 511145     DOI: 10.1007/bf00287173

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  28 in total

1.  Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.

Authors:  R H Lindenbaum; M Bobrow
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

2.  Balanced familial translocation t(5;19)(q12;p or q11) with phenotypical abnormalities in a girl.

Authors:  C Stoll; J M Levy; M Champy
Journal:  Humangenetik       Date:  1975

3.  Influence of time of mating on the segregation ratio of alleles at the T locus in the house mouse.

Authors:  A W BRADEN
Journal:  Nature       Date:  1958-03-15       Impact factor: 49.962

4.  Recurrent abortions and chromosome abnormalities.

Authors:  M Lucas; I Wallace; K Hirschhorn
Journal:  J Obstet Gynaecol Br Commonw       Date:  1972-12

5.  Structural variation in human nitotic chromosomes.

Authors:  J Leisti
Journal:  Ann Acad Sci Fenn Biol       Date:  1971

6.  Chromosome anomalies in three successive abortuses due to paternal translocation, t(13q-18q+).

Authors:  T Kajii; J Meylan; K Mikamo
Journal:  Cytogenet Cell Genet       Date:  1974

7.  Banding analysis of abnormal karyotypes in spontaneous abortion.

Authors:  T Kajii; K Oama; N Niikawa; A Ferrier; S Avirachan
Journal:  Am J Hum Genet       Date:  1973-09       Impact factor: 11.025

8.  A 3/4 reciprocal translocation in two unrelated families.

Authors:  M L Tenchini; E Montali; G Simoni; F Nuzzo
Journal:  Hum Genet       Date:  1977-06-30       Impact factor: 4.132

Review 9.  Sex-chromosome pairing and male fertility.

Authors:  G L Miklos
Journal:  Cytogenet Cell Genet       Date:  1974

10.  Centromeric effect on the degree of nonrandom disjunction in the female Drosophila melanogaster.

Authors:  H F Mark; S Zimmering
Journal:  Genetics       Date:  1977-05       Impact factor: 4.562

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  19 in total

1.  Direct segregation analysis of reciprocal translocations: a study of 283 sperm karyotypes from four carriers.

Authors:  F Pellestor; B Sèle; H Jalbert; P Jalbert
Journal:  Am J Hum Genet       Date:  1989-04       Impact factor: 11.025

2.  Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.

Authors:  J C Barber; C A Joyce; M N Collinson; J C Nicholson; L R Willatt; H M Dyson; M S Bateman; A J Green; J R Yates; N R Dennis
Journal:  J Med Genet       Date:  1998-06       Impact factor: 6.318

3.  A prenatal tertiary trisomy resulting from balanced maternal 8; 9 translocation.

Authors:  Gülsüm Kayhan; Mehmet Ali Ergün; Aydan Asyalı Biri; Meral Yirmibeş Karaoğuz
Journal:  J Turk Ger Gynecol Assoc       Date:  2011-09-01

Review 4.  Are double translocations double trouble?

Authors:  S M Bowser-Riley; M J Griffiths; M R Creasy; P A Farndon; K E Martin; D A Thomson; S A Larkins; R A Johnson; J L Watt
Journal:  J Med Genet       Date:  1988-05       Impact factor: 6.318

5.  Cytogenetics of recurrent spontaneous aborters.

Authors:  S P McManus; M A de Arce
Journal:  Ir J Med Sci       Date:  1986-07       Impact factor: 1.568

6.  Logistic regression model to estimate the risk of unbalanced offspring in reciprocal translocations.

Authors:  C Cans; O Cohen; C Lavergne; M A Mermet; J Demongeot; P Jalbert
Journal:  Hum Genet       Date:  1993-12       Impact factor: 4.132

7.  Segregation of a complex rearrangement of chromosomes 6, 7, 8, and 12 through three generations.

Authors:  B Meer; G Wolff; E Back
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

8.  Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height.

Authors:  T Ogata; N Matsuo
Journal:  Hum Genet       Date:  1993-07       Impact factor: 4.132

Review 9.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318

10.  Non random distribution of genomic features in breakpoint regions involved in chronic myeloid leukemia cases with variant t(9;22) or additional chromosomal rearrangements.

Authors:  Francesco Albano; Luisa Anelli; Antonella Zagaria; Nicoletta Coccaro; Paola Casieri; Antonella Russo Rossi; Laura Vicari; Vincenzo Liso; Mariano Rocchi; Giorgina Specchia
Journal:  Mol Cancer       Date:  2010-05-25       Impact factor: 27.401

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