{"title":"A subtelocentric chromosome 9 in a dysplastic 18-year-old boy with dissociated mental development.","authors":"I Hansmann, J Keutel","doi":"10.1007/BF00275140","DOIUrl":null,"url":null,"abstract":"<p><p>A subtelocentric C-group chromosome was identified as inv(9) (p24q12) in an 18-year-old young man who shows few dysplastic signs and who suffers from dissociated mental development. Pericentric inversions producing an almost metacentri No. 9 have been reported in several studies. The frequency of which proved to be high. There is an apparent lack, however, of inverted acro- or subtelocentric No. 9 reported in the literature. This obvious difference in the break points on chromosome 9 is most likely due to 1. hot-spots for chromosome breakage i.e. highly susceptible regions such as the euchromatic-heterochromatic junctions. 2. a higher degree of elimination against such acro- or subtelocentric chromosomes from one generation to the other.</p>","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"30 4","pages":"287-9"},"PeriodicalIF":0.0000,"publicationDate":"1975-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Humangenetik","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/BF00275140","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
A subtelocentric C-group chromosome was identified as inv(9) (p24q12) in an 18-year-old young man who shows few dysplastic signs and who suffers from dissociated mental development. Pericentric inversions producing an almost metacentri No. 9 have been reported in several studies. The frequency of which proved to be high. There is an apparent lack, however, of inverted acro- or subtelocentric No. 9 reported in the literature. This obvious difference in the break points on chromosome 9 is most likely due to 1. hot-spots for chromosome breakage i.e. highly susceptible regions such as the euchromatic-heterochromatic junctions. 2. a higher degree of elimination against such acro- or subtelocentric chromosomes from one generation to the other.