作者
M Fraccaro, J Lindsten, CE Ford, L Iselius, A Antonelli, P Aula, A Aurias, AD Bain, M Bartsch-Sandhoff, F Bernardi, E Boyd, LF Buchanan, AH Cameron, Albert de la Chapelle, G Ciuffa, C Cuoco, B Dutrillaux, G Dutton, MA Ferguson-Smith, D Francesconi, JPM Geraedts, G Gimelli, J Gueguen, E Gärsner, A Hagemeijer, FJ Hansen, PE Hollings, TWJ Hustinx, A Kaakinen, JJP van de Kamp, H von Koskull, J Lejeune, RH Lindenbaum, HH McCreanor, M Mikkelsen, F Mitelman, B Nicoletti, J Nilsby, B Nilsson, B Noel, E Padovani, F Pasquali, J de Pater, C Pedersen, F Petersen, EB Robson, J Rotman, M Ryynänen, E Sachs, J Salat, RH Smythe, I Stabell, I Šubrt, P Vampirelli, G Wessner, L Zergollern, O Zuffardi
发表日期
1980/10
期刊
Human genetics
卷号
56
页码范围
21-51
出版商
Springer-Verlag
简介
Translocation between the long arms of chromosomes 11 and 22 is usually detected in offspring with an unbalanced karyotype following a 3:1 disjunction resulting in “partial trisomy.” Since by the end of 1976 it was suspected that this translocation might be more frequent than one would deduce from published reports, it was decided to call for a collaborative effort in Europe to collect unpublished cases. In response, 42 cases were collected in Europe, and one case from New Zealand was added. The following countries were represented with the number of cases indicated in parentheses: Czechoslovakia (2), Denmark (4), Finland (3), France (6), Germany (1), Italy (5), The Netherlands (9), Sweden (6), United Kingdom (4), Yugoslavia (2). The wide geographical distribution indicates a multifocal origin of the translocation. Among the unpublished cases, 31 were ascertained as unbalanced carriers [47,XX or …
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M Fraccaro, J Lindsten, CE Ford, L Iselius, A Antonelli… - Human genetics, 1980