Urologia Internationalis
Original Paper
Cryptorchidism and Marker Chromosomes: Identification of Marker Chromosomes by Fluorescence in situ HybridizationSasagawa I. · Nakada T. · Ishigooka M. · Tomaru M. · Sawamura T. · Tateno T.Department of Urology, Yamagata University School of Medicine, Yamagata, Japan
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Article / Publication Details
Received: June 27, 1994
Accepted: December 07, 1994
Published online: February 03, 2010
Issue release date: 1995
Number of Print Pages: 4
Number of Figures: 0
Number of Tables: 0
ISSN: 0042-1138 (Print)
eISSN: 1423-0399 (Online)
For additional information: https://www.karger.com/UIN
Abstract
Identification of marker chromosomes by fluorescence in situ hybridization was performed in 2 cases of cryptorchidism. In case 1, the marker chromosome was derived from chromosome 22. In case 2, the origin of the marker was the centromere of chromosome 8. The extent of the congenital anomalies in these cases was milder than that in cases with complete trisomy of an autosome. These findings suggest that an incomplete extra autosome might influence clinical characteristics.
© 1995 S. Karger AG, Basel
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Article / Publication Details
Received: June 27, 1994
Accepted: December 07, 1994
Published online: February 03, 2010
Issue release date: 1995
Number of Print Pages: 4
Number of Figures: 0
Number of Tables: 0
ISSN: 0042-1138 (Print)
eISSN: 1423-0399 (Online)
For additional information: https://www.karger.com/UIN
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