11q trisomy detected by fluorescence in situ hybridization
Corresponding Author
Takako Takano
Departments of Hygiene & Public Health, Tokyo
MD, Department of Hygiene & Public Health, Teikyo University School of Medicine, 2–11-1 Kaga, Itabashi-ku, Tokyo 173, JapanSearch for more papers by this authorYasuko Yamanouchi
Departments of Hygiene & Public Health, Tokyo
Search for more papers by this authorShoko Kawashima
Pediatrics, Teikyo University School of Medicine, Tokyo
Search for more papers by this authorMasatsune Date
Pediatrics, Teikyo University School of Medicine, Tokyo
Search for more papers by this authorShintaro Hashira
Pediatrics, Teikyo University School of Medicine, Tokyo
Search for more papers by this authorMitsushiro Kida
Pediatrics, Teikyo University School of Medicine, Tokyo
Search for more papers by this authorToshiaki Abe
Pediatrics, Teikyo University School of Medicine, Tokyo
Search for more papers by this authorYutaka Nakahori
Department of Human Genetics, School of International Health, University of Tokyo, Tokyo, Japan
Search for more papers by this authorYasuo Nakagome
Department of Human Genetics, School of International Health, University of Tokyo, Tokyo, Japan
Search for more papers by this authorCorresponding Author
Takako Takano
Departments of Hygiene & Public Health, Tokyo
MD, Department of Hygiene & Public Health, Teikyo University School of Medicine, 2–11-1 Kaga, Itabashi-ku, Tokyo 173, JapanSearch for more papers by this authorYasuko Yamanouchi
Departments of Hygiene & Public Health, Tokyo
Search for more papers by this authorShoko Kawashima
Pediatrics, Teikyo University School of Medicine, Tokyo
Search for more papers by this authorMasatsune Date
Pediatrics, Teikyo University School of Medicine, Tokyo
Search for more papers by this authorShintaro Hashira
Pediatrics, Teikyo University School of Medicine, Tokyo
Search for more papers by this authorMitsushiro Kida
Pediatrics, Teikyo University School of Medicine, Tokyo
Search for more papers by this authorToshiaki Abe
Pediatrics, Teikyo University School of Medicine, Tokyo
Search for more papers by this authorYutaka Nakahori
Department of Human Genetics, School of International Health, University of Tokyo, Tokyo, Japan
Search for more papers by this authorYasuo Nakagome
Department of Human Genetics, School of International Health, University of Tokyo, Tokyo, Japan
Search for more papers by this authorAbstract
Takano T, Yamanouchi Y, Kawashima S, Date M, Hashira S, Kida M, Abe T, Nakahori Y, Nakagome Y. 11q trisomy detected by fluorescence in situ hybridization. Clin Genet 1993: 44: 324–328. © Munksgaard, 1993
A patient with psychomotor developmental delay, multiple minor anomalies, congenital heart disease and left inguinal hernia is reported. His karyotype was 45,X/46,X,+mar (3 : 37 cells), and the marker chromosome was identified as t(Y;11) (q12;q14?) using fluorescence in situ hybridization and fluorescent chromosome painting. He was diagnosed as mosaic for de novo 11q trisomy.
References
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