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pro vyhledávání: '"R. Coppieters"'
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Publikováno v:
Clinical Genetics. 22:37-39
A previously unpublished association of retinoblastoma and histiocytosis-X is described in a girl. In addition, chromosome analysis revealed a mosaicism of normal and abnormal mitoses. A deleted D-group chromosome (13q14-q31) was present.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a816d06287087c46857a63eb49077b3
https://doi.org/10.1111/j.1399-0004.1982.tb01408.x
https://doi.org/10.1111/j.1399-0004.1982.tb01408.x
Publikováno v:
English Studies. 60:835-840
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c6e74629126d4c6522969d46e6d7b7f
https://doi.org/10.1080/00138387908598019
https://doi.org/10.1080/00138387908598019
Autor:
R. Coppieters
Publikováno v:
English Studies. 59:589-592
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf4a379c6d4f50667b8184ef516adb4b
https://doi.org/10.1080/00138387808597934
https://doi.org/10.1080/00138387808597934
Publikováno v:
Ophthalmologica. 181:93-99
Radiogenic or non-radiogenic osteosarcomas were found in approximately 15% of the observed bilateral retinoblastoma cases, and only exceptionally in the unilateral cases. Such osteosarcomas are also seen in subjects without retinoblastoma, but belong
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b471d93be61fc5e0c853ae954ac2846
https://doi.org/10.1159/000309033
https://doi.org/10.1159/000309033
Autor:
A.O. Ramos, Shigeo Tsukahara, Y. Herishanu, S. Lavy, G. Ducel, A. Romano, R. Dufour, Magda Radnót, W. Paul, R. Coppieters, M. Hanssens, J. Littmann, M. Bücklers, S. Ishikawa, Susanne Richter, V.P.S. Tomar, P. Zlatar, R. Stein, Astré, D. Pajic, A. Magora, M. Dreifus, H. Zauberman, B. Lovas, a M. Giesbrecht, R. Praus, J. Bacskulin, E. Sakellaridès, C. Jönsas, P. Follmann, M. Tsacopoulos, P. Jobbágyi, I. Heszberger, S. Heszberger, V. Štambuk, A. de Rouck, I. Brettschneider, L. Ramos, O.P. Sharma, J. Collignon-Brach, L. Urai, G. de Crousaz, J. François, Y. Sato, R. Barishak, F. Tanner
Publikováno v:
Ophthalmologica. 159:I-VIII
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70e46bb55c3693c0c280d378e1bc83d1
https://doi.org/10.1159/000305958
https://doi.org/10.1159/000305958
Publikováno v:
Ophthalmologica. 102:129-137
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27cacb0279870b3dd808150adbc1df77
https://doi.org/10.1159/000299971
https://doi.org/10.1159/000299971
Publikováno v:
American Journal of Ophthalmology. 73:643-650
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b81bdaf7be288026e47de6a5d4b22a6
https://doi.org/10.1016/0002-9394(72)90378-9
https://doi.org/10.1016/0002-9394(72)90378-9
Publikováno v:
Acta geneticae medicae et gemellologiae. 18:18-50
SUMMARYThe malformative syndrome with cryptophthalmos is characterized by cryptophthalmos or congenital symblepharon of the upper lid, dyscephalia with malformations of the ears, nose and mouth, syndactylia, malformations of the urogenital organs and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07de7018fd18180c66a22ea92cf2764c
https://doi.org/10.1017/s1120962300012294
https://doi.org/10.1017/s1120962300012294
Autor:
Jules François, J. Scouras, G. Netter, R. Coppieters, O.S.B. Ferraz, W. Arkin, J. Piérard, L. Przondka, R. van Daele, Ahti Tarkkanen, B. Daicker, Anneli Klemetti, Olga Litričin
Publikováno v:
Ophthalmologica. 166:I-VI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::576caf163e039e5161759e3523e36640
https://doi.org/10.1159/000306912
https://doi.org/10.1159/000306912