Ann Genet. 1979;22(4):210-3.

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

[Article in French]

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

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.

PMID:: 317782; [PubMed - indexed for MEDLINE]

Publication Types, MeSH Terms

Publication Types

MeSH Terms

LinkOut - more resources

Supplemental Content

Save items

Related citations in PubMed

A new case of rearrangement of chromosome 15 associated with Prader Willi syndrome. [Clin Genet. 1980]
A new case of rearrangement of chromosome 15 associated with Prader Willi syndrome.
Guanti G. Clin Genet. 1980 Jun; 17(6):423-7.
Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population. [Am J Med Genet. 1984]
Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population.
Cassidy SB, Thuline HC, Holm VA. Am J Med Genet. 1984 Feb; 17(2):485-95.
Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome. [J Med Genet. 1997]
Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome.
Devriendt K, Petit P, Matthijs G, Vermeesch JR, Holvoet M, De Muelenaere A, Marynen P, Cassiman JJ, Fryns JP. J Med Genet. 1997 May; 34(5):395-9.
Review Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis. [Hum Genet. 1984]
Review Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.
Mattei MG, Souiah N, Mattei JF. Hum Genet. 1984; 66(4):313-34.
Review Nonreciprocal and jumping translocations of 15q1----qter in Prader-Willi syndrome. [Am J Med Genet. 1990]
Review Nonreciprocal and jumping translocations of 15q1----qter in Prader-Willi syndrome.
Rivera H, Zuffardi O, Gargantini L. Am J Med Genet. 1990 Nov; 37(3):311-7.

See reviews... See all...

Cited by 8 PubMed Central articles

Recurrent genomic instability of chromosome 1q in neural derivatives of human embryonic stem cells. [J Clin Invest. 2012]
Recurrent genomic instability of chromosome 1q in neural derivatives of human embryonic stem cells.
Varela C, Denis JA, Polentes J, Feyeux M, Aubert S, Champon B, Piétu G, Peschanski M, Lefort N. J Clin Invest. 2012 Feb 1; 122(2):569-74. Epub 2012 Jan 24.
Meiotic segregation and interchromosomal effect in the sperm of a double translocation carrier: a case report. [Mol Cytogenet. 2009]
Meiotic segregation and interchromosomal effect in the sperm of a double translocation carrier: a case report.
Juchniuk de Vozzi MS, Santos SA, Pereira CS, Cuzzi JF, Laureano LA, Franco JG Jr, Martelli L. Mol Cytogenet. 2009 Dec 1; 2:24. Epub 2009 Dec 1.
Definitive molecular cytogenetic characterization of 15 colorectal cancer cell lines. [Genes Chromosomes Cancer. 2010]
Definitive molecular cytogenetic characterization of 15 colorectal cancer cell lines.
Knutsen T, Padilla-Nash HM, Wangsa D, Barenboim-Stapleton L, Camps J, McNeil N, Difilippantonio MJ, Ried T. Genes Chromosomes Cancer. 2010 Mar; 49(3):204-23.

See all...

Related information

Related Citations
Calculated set of PubMed citations closely related to the selected article(s) retrieved using a word weight algorithm. Related articles are displayed in ranked order from most to least relevant, with the “linked from” citation displayed first.
Cited in PMC
Full-text articles in the PubMed Central Database that cite the current articles.

Recent activity

Clear Turn Off Turn On

[A jumping translocation (5p;15q), (8q;15q), and (12q;15q) (author's transl)].
[A jumping translocation (5p;15q), (8q;15q), and (12q;15q) (author's transl)].
Ann Genet. 1979 ;22(4):210-3.

PubMed
Trisomy 21 Down syndrome. Parental mosaicism.
Trisomy 21 Down syndrome. Parental mosaicism.
Hum Genet. 1985 ;70(3):246-8.

PubMed
Rapid speciation and chromosomal evolution in mammals.
Rapid speciation and chromosomal evolution in mammals.
Proc Natl Acad Sci U S A. 1977 Sep ;74(9):3942-6.

PubMed
[Penta-X syndrome. Report of a case with 47,XXX/48,XXXX/49,XXXXX mosaicism].
[Penta-X syndrome. Report of a case with 47,XXX/48,XXXX/49,XXXXX mosaicism].
Bol Med Hosp Infant Mex. 1989 Jun ;46(6):417-21.

PubMed
High rates of de novo 15q11q13 inversions in human spermatozoa.
High rates of de novo 15q11q13 inversions in human spermatozoa.
Mol Cytogenet. 2012 Feb 6 ;5(1):11.

PubMed

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

PubMed

Result Filters

Display Settings:

Send to:

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

Abstract

Publication Types, MeSH Terms

Publication Types

MeSH Terms

LinkOut - more resources

Other Literature Sources

Medical

Libraries

Supplemental Content

Save items

Related citations in PubMed

Cited by 8 PubMed Central articles

Related information

Recent activity

Simple NCBI Directory

Getting Started

Resources

Popular

Featured

NCBI Information