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Familial reciprocal translocation t(9;13)(p11;p12) investigated by silver staining and in situ hybridisation
Authors:Jennifer M. Varley  John Gosden  Maj Hultén
Affiliation:(1) Department of Zoology, School of Biological Sciences, University of Leicester, LE1 7RH Leicester, UK;(2) MRC Clinical and Population Cytogenetics Unit, Western General Hospital, Crewe Road, EH4 2XU Edinburgh, UK;(3) Regional Cytogenetics Laboratory, East Birmingham Hospital, Bordesley Green East, B9 5ST Birmingham, UK
Abstract:Summary A maternal de novo reciprocal translocation between the short arms of chromosomes 9 and 13 is reported. Using C-, Q- or G-banding, it was not possible to determine the precise breakpoint on 13, but a combination of silver staining and in situ hybridisation was used to do so on the two chromosomes, and it was demonstrated that the break on chromosome 13 had occurred within the NOR.
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