Zobrazeno 1 - 10
of 202
pro vyhledávání: '"Brecevic, L"'
Autor:
Guilherme R.S., Klein E, Hamid A.B., Bhatt S, Volleth M, Polityko A, Kulpanovich A, Dufke A, Albrecht B, Morlot S, Brecevic L, Petersen M.B., Manolakos E, Kosyakova N, Liehr T
Publikováno v:
Balkan Journal of Medical Genetics, Vol 16, Iss 1, Pp 13-19 (2013)
Twenty-nine as yet unreported ring chromosomes were characterized in detail by cytogenetic and molecular techniques. For FISH (fluorescence in situ hybridization) previously published high resolution approaches such as multicolor banding (MCB), subce
Externí odkaz:
https://doaj.org/article/dd623083f5084a18b23460c1fd9f5a9b
Publikováno v:
In European Journal of Medical Genetics 2011 54(2):152-156
Autor:
Liehr T, Trifonov V, Polityko A, Brecevic L, Mrasek K, Weise A, Ewers E, Reich D, Iourov I, Mkrtchyan H, Manvelyan M, Kosyakova N
Publikováno v:
Balkan Journal of Medical Genetics, Vol 10, Iss 1, Pp 33-37 (2007)
Externí odkaz:
https://doaj.org/article/84a8e52c52884baa823b2a88aac69e9a
Autor:
Kummer, I., Drzaic, M., Iva Buzancic, Marusic, M., Butkovic, D., Kolaric, M., Jurinic, H., Matkovic, M., Brecevic, L., Bursic, T., Hadziabdic, M. Ortner, Brkic, J., Fialova, D.
Publikováno v:
Publons
Web of Science
Web of Science
Background and Objective: The aim of the study was to determine the health and nutritional status of the Croatian older population visiting community pharmacies, using the methods of comprehensive geriatric assessment. Setting and Method: The researc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::89e59d2a26a613774452866876aef6d5
https://www.bib.irb.hr/1253485
https://www.bib.irb.hr/1253485
Autor:
Weise, A, Kosyakova, N, Mrasek, K, Ewers, E, Bacino, C, Patel, A, Cheung, SW, Cai, WW, Senger, G, Melo, JB, Carreira, IM, Dufke, A, Mehnert, K, Yardin, C, Wegner, RD, Stumm, M, Kistner, G, Leipoldt, M, Thiel, G, Petersen, MB, Junge, A, Fritz, B, Joksic, G, Heilbronner, H, Ujfalusi, A, Brecevic, L, Hamid, AB, Merkas, M, Liehr, T.
Array-comparative genomic hybridization (aCGH) was done in 64 small supernumerary marker chromosomes (sSMC). The studied sSMC-specific DNA was derived from glass-needle based microdissection, avoiding by that the problem of mosaicism as present in ~4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::e4d3b311f7b1344c3ccbe0b89c0ee914
https://www.bib.irb.hr/461160
https://www.bib.irb.hr/461160
Autor:
Wagner, J, Dorner, S, Stipoljev, F, Skrlec, I, Lauc, G, Weise, A, Mrasek, K, Liehr, T, Brecevic, L
Phenotype in patients with segmental aneuploidy often vary in their clinical manifestation depending on the size of the chromosomal region involved. Deletions of chromosome regions 4q31, 4q32, and 4q33-4qter lead to a distinctive malformation syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::b60287fce2de8bb826dfc2d763599adb
https://www.bib.irb.hr/461632
https://www.bib.irb.hr/461632
Introduction: Small supernumerary marker chromosomes (sSMC) are present in 0.043% of newborn. In about 30% of sSMC carriers an abnormal phenotype is observed. Clinical outcome of sSMC presence is difficult to predict as different phenotypic consequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::65ae1282e652582ddedf40fd4f213724
https://www.bib.irb.hr/282112
https://www.bib.irb.hr/282112
Introduction: Small supernumerary marker chromosomes (sSMC) are present in 0.043% of newborn. In about 30% of sSMC carriers an abnormal phenotype is observed. Clinical outcome of sSMC presence is difficult to predict as different phenotypic consequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::e188ddfe9d2cf38654e09d383b15aeba
https://www.bib.irb.hr/282162
https://www.bib.irb.hr/282162
There are only about 30 commercially available cell lines which include small supernumerary marker chromosomes (sSMC). As approximately 2.5 million people worldwide are carriers of an sSMC, this small number of immortalized cell lines is hard to unde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::7687546570660ccd35c7f822b1f211be
https://www.bib.irb.hr/282200
https://www.bib.irb.hr/282200
Publikováno v:
International Journal of Oncology.
Hematopoietic disorders can be used as a suitable tool of additional information on the actual resolving power of comparative genomic hybridization (CGH). Therefore, CGH examination was performed of DNA extracted from 23 acute and 15 chronic myelopro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c414395b3fe106d0cc84cdd39b6f57b0
https://doi.org/10.3892/ijo.16.6.1099
https://doi.org/10.3892/ijo.16.6.1099