Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Oberle, I."'
Autor:
Oberlé, I., Heilig, R., Moisan, J. P., Kloepfer, C., Mattéi, M. G., Mattéi, J. F., Boué, J., Froster-Iskenius, U., Jacobs, P. A., Lathrop, G. M., Lalouel, J. M., Mandel, J. L.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1986 Feb . 83(4), 1016-1020.
Externí odkaz:
https://www.jstor.org/stable/27085
Autor:
de Saint Basile, G., Arveiler, B., Oberlé, I., Malcolm, S., Levinsky, R. J., Lau, Y. L., Hofker, M., Debre, M., Fischer, A., Griscelli, C., Mandel, J. L.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1987 Nov 01. 84(21), 7576-7579.
Externí odkaz:
https://www.jstor.org/stable/30866
Autor:
Heitz, D., Rousseau, F., Devys, D., Saccone, S., Abderrahim, H., Le Paslier, D., Cohen, D., Vincent, A., Toniolo, D., Della Valle, G., Johnson, S., Schlessinger, D., Oberle, I., Mandel, J. L.
Publikováno v:
Science, 1991 Mar 01. 251(4998), 1236-1239.
Externí odkaz:
https://www.jstor.org/stable/2875314
Autor:
Oberlé, I., Rousseau, F., Heitz, D., Kretz, C., Devys, D., Hanauer, A., Boué, J., Bertheas, M. F., Mandel, J. L.
Publikováno v:
Science, 1991 May . 252(5009), 1097-1102.
Externí odkaz:
https://www.jstor.org/stable/2876286
Autor:
Gk, Suthers, Valentine Hyland, Df, Callen, Oberle I, Rocchi M, Ns, Thomas, Cp, Morris, Ce, Schwartz, Schmidt M, Hh, Ropers
Publikováno v:
Europe PubMed Central
The fragile X syndrome is a very common disorder, but there has been little progress toward isolating the fragile X mutation (FRAXA). We describe a panel of 14 somatic cell hybrid lines, lymphoblastoid cell lines, and peripheral lymphocytes with X-ch
Autor:
Tommerup, N., Søndergaard, F., Hanauer, A., Oberle, I., Bang, J., Barbi, B., Bech, B., Davies, K., Froster-Iskenius, U., Gustavson, K.-H., van der Hagen, C. B., Heiberg, A., Kristoffersen, U., Mikkelsen, M., Miny, P., Nielsen, K. B., Rasmussen, K., Schinzel, A., Tranebjaerg, L., Tønnesen, T.
Publikováno v:
Prenatal Diagnosis; Aug1991, Vol. 11 Issue 8, p609-619, 11p
Publikováno v:
Human Genetics; 1986, Vol. 74 Issue 4, p391-398, 8p
Autor:
Suthers, G. K., Hyland, V. J., David Callen, Oberle, I., Rocchi, M., Thomas, N. S., Morris, C. P., Schwartz, C. E., Schmidt, M., Ropers, H. H., Baker, E., Oostra, B. A., Dahl, N., Wilson, P. J., Hopwood, J. J., Sutherland, G. R.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4c7445f1694d1368df6059103293213d
http://www.scopus.com/inward/record.url?eid=2-s2.0-0025030304&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0025030304&partnerID=MN8TOARS
Autor:
Rousseau, F., Vincent, A., Stefano Rivella, Heitz, D., Triboli, C., Maestrini, E., Warren, S. T., Suthers, G. K., Goodfellow, P., Mandel, J. L., Toniolo, D., Oberle, I.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6a5e956e193402ac40e420fded164fb4
http://www.scopus.com/inward/record.url?eid=2-s2.0-0026068620&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0026068620&partnerID=MN8TOARS