Literature DB >> 395305

Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations.

P Jalbert, B Sele.   

Abstract

Reciprocal translocations produce imbalances by three types of disjunction which are, in decreasing frequency, adjacent 1, 3:1, and adjacent 2. Adjacent 1 disjunction produces duplication deficiencies of inverse topography to those of adjacent 2. The imbalanced chromosome segments in one of these types are balanced in the other. The disjunction 3:1 produces pure trisomies and monosomies. The following situations predispose to adjacent 2 disjunction: translocations between the long arms of two acrocentric chromosomes or between one of these and that of a No 9 chromosome; centric segments, either short or carrying a heterochromatic zone (9qh); a balanced translocation in the mother. The factors predisposing to the disjunction adjacent 2 operate by selection, or directly on the meiotic configuration. Some of them (shortness of the interstitial segment, shortness of the short arms of translocation chromosomes) act in both these ways. Their influence is probably responsible for the repetitive and exclusive character of this disjunction. The conditions for the occurrence of the 3:1 disjunctions seem less strict than those for adjacent 2, although they should be of the same nature (involvement of acrocentrics or a chromosome 9 in the translocation, maternal origin).

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Year:  1979        PMID: 395305      PMCID: PMC1012595          DOI: 10.1136/jmg.16.6.467

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


  144 in total

1.  PARTIAL TRISOMY-DEFICIENCY SYNDROME RESULTING FROM A RECIPROCAL TRANSLOCATION IN A LARGE KINDRED.

Authors:  I A UCHIDA; H C WANG; O E LAXDAL; W A ZALESKI; B P DUNCAN
Journal:  Cytogenetics       Date:  1964

2.  Partial trisomy 20 (20q13) and partial trisomy 21 (21pter leads to 21q21.3).

Authors:  O Sanchéz; P Mamunes; J J Yunis
Journal:  J Med Genet       Date:  1977-12       Impact factor: 6.318

3.  Trisomy 9p and unusual translocation mongolism in siblings due to different 3:1 segregations of maternal translocation rcp(9;21)(p11;q11).

Authors:  M Habedank; J Faust
Journal:  Hum Genet       Date:  1978-06-27       Impact factor: 4.132

4.  Partial trisomies of chromosome 21 in man. Two new observations due to translocations 19;21 and 4;21.

Authors:  R A Pfeiffer; E K Kessel; K H Soer
Journal:  Clin Genet       Date:  1977-03       Impact factor: 4.438

5.  [Partial trisomy of chromosome 21 by maternal translocation t(15;21) (q26.2; q21)].

Authors:  O Raoul; S Carpentier; B Dutrillaux; R Mallet; J Lejeune
Journal:  Ann Genet       Date:  1976-09

6.  Chromosome segregation in translocations involving chromosome 6 in maize.

Authors:  C R BURNHAM
Journal:  Genetics       Date:  1950-07       Impact factor: 4.562

7.  [Partial trisomy 10p of paternal origin. 2 new cases in 2 different families].

Authors:  M Rolland; G Bourrouillou; G Elana; P Colombies; C Regnier
Journal:  Ann Genet       Date:  1977-09

8.  Partial trisomy 18(q11 leads to qter) in an infant and aborted fetus resulting from a balanced paternal translocation t(13;18)(q32:q11).

Authors:  A Rosenmann; M Isacson; R Cohen; M Segal; M M Cohen
Journal:  Ann Genet       Date:  1978-03

9.  Partial trisomy 10p in two generations.

Authors:  I W Lurie; G I Lazjuk; D B Gurevich; G I Kravtzoa; M K Nedzved; I A Shved
Journal:  Hum Genet       Date:  1978-03-17       Impact factor: 4.132

10.  Trisomy 12p syndrome. Evaluation of a family with a t(12;21) (p12.1;p11) translocation with unbalanced offspring.

Authors:  I L Hansteen; L Schirmer; S Hestetun
Journal:  Clin Genet       Date:  1978-04       Impact factor: 4.438

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  14 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.  Human sperm chromosome studies in a reciprocal translocation t(2;5).

Authors:  C Templado; J Navarro; J Benet; A Genescà; M M Pérez; J Egozcue
Journal:  Hum Genet       Date:  1988-05       Impact factor: 4.132

3.  Segregation analysis of translocations by the study of human sperm chromosome complements.

Authors:  R H Martin
Journal:  Am J Hum Genet       Date:  1989-04       Impact factor: 11.025

4.  Maternal 3:1 disjunction in a translocation 9/17.

Authors:  M A Sánchez Ferrer; M L de Torres; J A Abrisqueta
Journal:  Hum Genet       Date:  1986-06       Impact factor: 4.132

5.  Human reciprocal translocations: is the unbalanced mode at birth predictable?

Authors:  C Cans; O Cohen; M A Mermet; J Demongeot; P Jalbert
Journal:  Hum Genet       Date:  1993-04       Impact factor: 4.132

Review 6.  Viability thresholds for partial trisomies and monosomies. A study of 1,159 viable unbalanced reciprocal translocations.

Authors:  O Cohen; C Cans; M A Mermet; J Demongeot; P Jalbert
Journal:  Hum Genet       Date:  1994-02       Impact factor: 4.132

7.  Chromosome abnormality in couples with histories of multiple abortions. The outcome of pregnancies subsequent to ascertainment and a study of familial translocation carriers.

Authors:  J Wolstenholme; M J Faed; J Robertson; M A Lamont
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

8.  Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing.

Authors:  P Jalbert; B Sele; H Jalbert
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

9.  Adjacent 2 translocation involving 13q and 21q.

Authors:  W W Woolf; C L Bradshaw; H E Hoyme; K L Jones; O W Jones
Journal:  J Med Genet       Date:  1982-08       Impact factor: 6.318

10.  Meiotic analysis by FISH of a human male 46,XY,t(15;20)(q11.2;q11.2) translocation heterozygote: quadrivalent configuration, orientation and first meiotic segregation.

Authors:  A S Goldman; M A Hultén
Journal:  Chromosoma       Date:  1993-01       Impact factor: 4.316

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