Literature DB >> 317782

[A jumping translocation (5p;15q), (8q;15q), and (12q;15q) (author's transl)].

J Lejeune, C Maunoury, M Prieur, J Van den Akker.   

Abstract

Three balanced karyotypes (5p;15q), (8q;15q), and (12q;15q) were found simultaneously in a child with the Willi-Prader syndrome. The hypothesis is presented of a "jumping# translocation by affinity of telomeric and interstitial palindromes. The relationship between the Willi-Prader syndrome and a juxtacentric anomaly of the long arm of chromosome 15 is discussed.

Entities:  

Mesh：

Year:  1979        PMID： 317782

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  20 in total

1.  Recurrent genomic instability of chromosome 1q in neural derivatives of human embryonic stem cells.

Authors:  Christine Varela; Jérôme Alexandre Denis; Jérôme Polentes; Maxime Feyeux; Sophie Aubert; Benoite Champon; Geneviève Piétu; Marc Peschanski; Nathalie Lefort
Journal:  J Clin Invest       Date:  2012-01-24       Impact factor: 14.808

2.  Isolation and analysis of DNA markers specific to human chromosome 15.

Authors:  D M Tasset; J A Hartz; F T Kao
Journal:  Am J Hum Genet       Date:  1988-06       Impact factor: 11.025

3.  Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes.

Authors:  T A Donlon
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

4.  Jumping translocations, a novel finding in chronic lymphocytic leukaemia.

Authors:  Cecelia R Miller; Deborah Stephens; Amy S Ruppert; Frederick Racke; Andrew McFaddin; Heather Breidenbach; Huey-Jen Lin; Kathy Waller; Tammy Bannerman; Jeffrey A Jones; Jennifer A Woyach; Leslie A Andritsos; Kami Maddocks; Weiqiang Zhao; Gerard Lozanski; Joseph M Flynn; Michael Grever; John C Byrd; Nyla A Heerema
Journal:  Br J Haematol       Date:  2015-04-19       Impact factor: 6.998

5.  A de novo satellited short arm of the Y chromosome possibly resulting from an unstable translocation.

Authors:  C L Lin; L Gibson; B Pober; T L Yang-Feng
Journal:  Hum Genet       Date:  1995-11       Impact factor: 4.132

6.  Unstable familial translocations: A t(11;22)mat inherited as a t(11;15).

Authors:  D J Tomkins
Journal:  Am J Hum Genet       Date:  1981-09       Impact factor: 11.025

Review 7.  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

8.  Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment.

Authors:  M Fraccaro; O Zuffardi; E Bühler; A Schinzel; G Simoni; R Witkowski; E Bonifaci; D Caufin; G Cignacco; N Delendi
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

9.  Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases.

Authors:  J F Mattei; M G Mattei; F Giraud
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

10.  Definitive molecular cytogenetic characterization of 15 colorectal cancer cell lines.

Authors:  Turid Knutsen; Hesed M Padilla-Nash; Danny Wangsa; Linda Barenboim-Stapleton; Jordi Camps; Nicole McNeil; Michael J Difilippantonio; Thomas Ried
Journal:  Genes Chromosomes Cancer       Date:  2010-03       Impact factor: 5.006
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