MOLECULAR ANALYSIS OF AN UNBALANCED DELETION OF THE SHORT ARM OF CHROMOSOME-5 THAT PRODUCES NO PHENOTYPE
- 1 July 1986
- journal article
- research article
- Vol. 39 (1) , 1-10
Abstract
A family has been identified in which an interstitial, apparently unbalanced deletion of the short arm of chromosome 5 could be traced through six individuals in 3 generations. Remarkably, all of the individuals with the deletion are completely asymptomatic and show no physical or mental abnormalities. The deletion was confirmed at the molecular level by identifying DNA probes that mapped within the deleted portion of chromosome 5. Through the use of somatic cell hybrids and quantitative Southern blots, we demonstrated that these individuals do indeed have an unbalanced deletion and are haploid for several million base pairs of DNA in 5p14 without showing any discernable phenotype.This publication has 21 references indexed in Scilit:
- Detection of specific sequences among DNA fragments separated by gel electrophoresisPublished by Elsevier ,2006
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1983
- Clinical heterogeneity in 80 home-reared childrenwith cri du chat syndromeThe Journal of Pediatrics, 1983
- Characterization of Giemsa dark- and light-band DNACell, 1982
- Selective linkage disruption in human-Chinese hamster cell hybrids: deletion mapping of the leuS, hexB, emtB, and chr genes on human chromosome 5.Molecular and Cellular Biology, 1982
- [27] KaryotypingPublished by Elsevier ,1979
- [26] A sensitive and rapid method for recombinant phage screeningPublished by Elsevier ,1979
- Hot spots and functional organization of human chromosomesHuman Genetics, 1978
- The cri du chat syndromeHuman Genetics, 1978
- Localization of sequences specifying messenger RNA to light-staining G-bands of human chromosomesChromosoma, 1977