Literature DB >> 7450764

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

P Jalbert, B Sele, H Jalbert.   

Abstract

The study of 151 reciprocal translocations associated with abnormal probands shows that the mode of imbalance at birth is determined by the nature of the involved chromosomes and by the position of the breakpoints. For each of the three modes (adjacent-1, adjacent-2, and 3:1) there is a corresponding pachytene diagram, so that for each translocation variety it is possible to predict the most probable mode of imbalance. The determining factor is the relative length of the different branches of the cross formed by the tetravalent. However, some heterochromatic regions (9qh, short arms of acrocentric chromosomes) and possibly R-negative regions have a minor role. The factors involved in these mechanisms seem to be the selection and the chiasma position; their respective roles are discussed.

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Year:  1980        PMID: 7450764     DOI: 10.1007/bf00291769

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


  141 in total

1.  [2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)].

Authors:  S Morić-Petrović; Z Laća; A Krajgher; J Milośevic
Journal:  Ann Genet       Date:  1976-09

2.  [Partial trisomy 11q and familial translocation 11--22 (author's transl)].

Authors:  F Giraud; J F Mattei; M G Mattei; R Bernard
Journal:  Humangenetik       Date:  1975-08-25

3.  Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9.

Authors:  C E Blank; D C Colver; A M Potter; J McHugh; J Lorber
Journal:  Clin Genet       Date:  1975-04       Impact factor: 4.438

4.  [Partial trisomy for the distal part of the short branch of chromosome 3].

Authors:  F Ballesta; L Vehi
Journal:  Ann Genet       Date:  1974-12

5.  Partial 7q trisomy.

Authors:  R Berger; C Turc; H Wachter; G Begue
Journal:  Clin Genet       Date:  1977-01       Impact factor: 4.438

6.  Partial trisomy-5p.

Authors:  E Yunis; R Silva; H Egel; R Zúñiga; O M Torres de Caballero; E Ramirez; H Poveda de Ruiz
Journal:  Hum Genet       Date:  1978-08-31       Impact factor: 4.132

7.  t(9/22) with centric fission and NOR translocation leading to a case of pure 9p trisomy in the offspring.

Authors:  N Archidiacono; M Rocchi; U de Vonderweid; G Filippi
Journal:  Hum Genet       Date:  1978-02-16       Impact factor: 4.132

8.  Mental retardation with 45 chromosomes 45,XX,--5,--14,+der(5) t(5,14)(p15;q13) mat due to familial balanced reciprocal translocation.

Authors:  K Fried; M Tieder; S Beer; M Rosenblatt; H I Krespin
Journal:  J Med Genet       Date:  1977-02       Impact factor: 6.318

9.  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

10.  [Familial translocation 3/22 MAT with partial trisomy 3q (author's transl)].

Authors:  G Schwanitz; R D Schmid; G Grosse; E Grahn-Liebe
Journal:  J Genet Hum       Date:  1977-06
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  37 in total

1.  Fluorescence in situ hybridisation (FISH) analysis of chromosome segregation and interchromosomal effect in spermatozoa of a reciprocal translocation t(9,10)(q11;p11.1) carrier.

Authors:  Nathalie Rives; Marion Jarnot; Nathalie Mousset-Siméon; Géraldine Joly; Bertrand Macé
Journal:  J Hum Genet       Date:  2003-10-02       Impact factor: 3.172

2.  Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis.

Authors:  K Mangelschots; B Van Roy; F Speleman; N Van Roy; J Gheuens; J Beuten; I Buntinx; M N Van Thienen; H Willekens; J Dumon
Journal:  Hum Genet       Date:  1992-06       Impact factor: 4.132

3.  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

4.  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

5.  Preimplantation genetic diagnosis for couples at high risk of Down syndrome pregnancy owing to parental translocation or mosaicism.

Authors:  C M Conn; J Cozzi; J C Harper; R M Winston; J D Delhanty
Journal:  J Med Genet       Date:  1999-01       Impact factor: 6.318

6.  Analysis using dual-colour fluorescence in situ hybridization of meiotic chromosome segregation in male mice heterozygous for a reciprocal translocation.

Authors:  C Tease
Journal:  Chromosome Res       Date:  1996-01       Impact factor: 5.239

7.  Bayesian Assessment of Genetic Risk in Families with a Balanced Translocation.

Authors:  Douglas VanDerwerken
Journal:  J Genet Couns       Date:  2015-02-04       Impact factor: 2.537

8.  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

9.  Fragile sites and breakpoints in constitutional rearrangements and in human sperm chromosomes.

Authors:  C Fuster; R Miró; C Templado; L Barrios; V Moreno; J Egozcue
Journal:  Hum Genet       Date:  1989-07       Impact factor: 4.132

Review 10.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

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