Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Boteva, Kalina"'
Autor:
Lieberman, Jeffrey A. *, Perkins, Diana, Belger, Aysenil, Chakos, Miranda, Jarskog, Fred, Boteva, Kalina, Gilmore, John
Publikováno v:
In Biological Psychiatry 2001 50(11):884-897
Autor:
Constantinou-Deltas, Constantinos D., Papageorgiou, Elena, Boteva, Kalina, Christodoulou, Kyproula, Breuning, M. H., Peters, D. J. M., Pierides, Alkis M.
Publikováno v:
Human genetics
Hum.Genet.
Hum.Genet.
Polycystic kidney disease is an inherited heterogeneous disorder that affects approximately 1:1000 Europeans. It is characterized mainly by the formation of cysts in the kidney that lead to end-stage renal failure with late age of onset. Three loci h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::614d5bd032a8867bad7a32b00ec18f52
http://gnosis.library.ucy.ac.cy/handle/7/53029
http://gnosis.library.ucy.ac.cy/handle/7/53029
Autor:
Constantinou-Deltas, Constantinos D., Papageorgiou, Elena, Boteva, Kalina, Christodoulou, Kyproula, Pierides, Alkis M.
Publikováno v:
Contributions to nephrology
Contrib.Nephrol.
Contrib.Nephrol.
115 93 96
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4485::660acd4363042d3cd0b39b81129e3f83
http://gnosis.library.ucy.ac.cy/handle/7/53030
http://gnosis.library.ucy.ac.cy/handle/7/53030
Autor:
Boteva, Kalina, Papageorgiou, Elena, Georgiou, Christina, Angastiniotis, Michael A., Middleton, Lefkos T., Constantinou-Deltas, Constantinos D.
Publikováno v:
Human genetics
Hum.Genet.
Hum.Genet.
Cyprus is an island in the eastern Mediter-ranean basin inhabited by people of Caucasian extraction, mostly Greek-Cypriots. The most common inherited disease among Caucasians is cystic fibrosis (CF). Although no careful scientific study had ever been
Autor:
Angelicheva, D., Boteva, Kalina, Jordanova, A., Savov, A., Kufardjieva, A., Tolun, A., Telatar, M., Akarsubaşi, A., Köprübaşi, F., Aydoǧdu, S., Demirkol, M., Kurdoǧlu, G., Constantinou-Deltas, Constantinos D., Georgiou, Christina, Dean, M., Ivaschenko, T., Baranov, V., Kalaydjieva, L.
Publikováno v:
Human mutation
Hum.Mutat.
Hum.Mutat.
A 2 bp deletion in exon 10 of the CFTR gene, 1677delTA, which is very rare among CF chromosomes worldwide, was found to be a relatively common cause of cystic fibrosis in countries located in the region of the Black Sea. The frequency of the mutation
Publikováno v:
American Journal of Psychiatry; Oct2005, Vol. 162 Issue 10, p1785-1804, 20p
Autor:
Boteva, Kalina, Lieberman, Jeffrey
Publikováno v:
World Journal of Biological Psychiatry; 2003, Vol. 4 Issue 2, p81-92, 12p
Autor:
Constantinou-Deltas, C., Papageorgiou, Elena, Boteva, Kalina, Christodoulou, Kyproula, Breuning, Martijn, Peters, D., Pierides, Alkis
Publikováno v:
Human Genetics; 1995, Vol. 95 Issue 4, p416-423, 8p
Autor:
Deltas, Constantinou C., Boteva, Kalina, Georgiou, Andreas, Papageorgiou, Elena, Georgiou, Christina
Publikováno v:
Molecular and Cellular Probes; August, 1996, Vol. 10 Issue: 4 p315-318, 4p
Autor:
Chu, Fong-Fong, Rohan de Silva, H.A., Esworthy, R.Steven, Boteva, Kalina K., Walters, Claire E., Roses, Allen, Rao, P.Nagesh, Pettenati, Mark J.
Publikováno v:
Genomics; March 1996, Vol. 32 Issue: 2 p272-276, 5p