Literature DB >> 6463033

A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses.

A Boué, P Gallano.   

Abstract

A collaborative study involving 71 European prenatal diagnosis centres has collected 1356 observations on the karyotype of fetal cells in diagnoses performed in couples in which a parent had a balanced structural rearrangement. The segregations of the inherited chromosome structural rearrangement were analysed in relation to the types of rearrangement, to the sex of the carrier parent, the methods of ascertainment of the anomaly in the family, the chromosomes involved and the potential imbalance of the anomaly. Wide differences in the incidence of unbalanced fetuses were observed in relation to these criteria, and these results can be used in counselling parents with balanced rearrangements. Distortions in segregation of normal versus balanced karyotypes were observed in some types of anomalies.

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Year:  1984        PMID: 6463033     DOI: 10.1002/pd.1970040705

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  43 in total

1.  Sperm chromosome analysis of two males heterozygous for a t(2;17)(q35;p13) and t(3;8)(p13;p21) reciprocal translocation.

Authors:  J Jenderny
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

Review 2.  The critical region on the human Xq.

Authors:  E Therman; R Laxova; B Susman
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

3.  Cytogenetic analysis of 400 sperm from three translocation heterozygotes.

Authors:  R H Martin; L Barclay; K Hildebrand; E Ko; S B Fowlow
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

4.  Preimplantation genetic haplotyping a new application for diagnosis of translocation carrier's embryos- preliminary observations of two robertsonian translocation carrier families.

Authors:  Jana Shamash; Shlomit Rienstein; Haike Wolf-Reznik; Elon Pras; Michal Dekel; Talia Litmanovitch; Masha Brengauz; Boleslav Goldman; Hagith Yonath; Jehoshua Dor; Jacob Levron; Ayala Aviram-Goldring
Journal:  J Assist Reprod Genet       Date:  2010-09-25       Impact factor: 3.412

5.  Indications for cytogenetic studies.

Authors:  Q H Qazi
Journal:  Indian J Pediatr       Date:  1989 Jul-Aug       Impact factor: 1.967

6.  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

7.  The segregation of a translocation t(1;4) in two male carriers heterozygous for the translocation.

Authors:  A M Estop; F Levinson; K Cieply; V Vankirk
Journal:  Hum Genet       Date:  1992-06       Impact factor: 4.132

8.  Cartographic study: breakpoints in 1574 families carrying human reciprocal translocations.

Authors:  O Cohen; C Cans; M Cuillel; J L Gilardi; H Roth; M A Mermet; P Jalbert; J Demongeot
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

9.  Breakpoint mapping and haplotype analysis of three reciprocal translocations identify a novel recurrent translocation in two unrelated families: t(4;11)(p16.2;p15.4).

Authors:  N Simon Thomas; Viv Maloney; Victoria Bryant; Shuwen Huang; Carole Brewer; Katherine Lachlan; Patricia A Jacobs
Journal:  Hum Genet       Date:  2008-12-24       Impact factor: 4.132

10.  Preconceptional diagnosis for Robertsonian translocation as an alternative to preimplantation genetic diagnosis in two situations: a pilot study.

Authors:  D Molina Gomes; I Hammoud; M Bailly; M Bergere; R Wainer; J Selva; F Vialard
Journal:  J Assist Reprod Genet       Date:  2009-01-28       Impact factor: 3.412

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