Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Anna I, Kulpanovich"'
Autor:
Lukrecija Brecevic, Roberta Santos Guilherme, Samarth Bhatt, Beate Albrecht, A Polityko, Anna I. Kulpanovich, Marianne Volleth, Michael B. Petersen, E Klein, Emmanouil Manolakos, Thomas Liehr, Ahmed B. Hamid, Nadezda Kosyakova, Andreas Dufke, Susanne Morlot
Publikováno v:
Balkan Journal of Medical Genetics : BJMG
Balkan Journal of Medical Genetics, Vol 16, Iss 1, Pp 13-19 (2013)
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8b7f22a028577849e84643f25ca7217
https://doi.org/10.2478/bjmg-2013-0013
https://doi.org/10.2478/bjmg-2013-0013
Autor:
Anja Weise, Konstantin A. Mosse, Natalia Rumyantseva, Irina Naumchik, Thomas Liehr, A Polityko, Olga M. Khurs, Anna I. Kulpanovich, Hasmik Mkrtchyan, Angelica V. Solntsava
Publikováno v:
European Journal of Medical Genetics. 52:207-210
An unusual mosaic karyotype was detected in a 6-year-old female patient with clinical diagnosis of Turner syndrome (TS). Cytogenetic and molecular cytogenetic studies revealed besides a cell line with 45,X a second cell line where the short arm of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9799f0564a2120cd7acc40ab949df476
https://doi.org/10.1016/j.ejmg.2009.03.016
https://doi.org/10.1016/j.ejmg.2009.03.016
Autor:
Emel Ergul, Martina Merkas, A Polityko, Gisela Reising-Ackermann, Marianne Volleth, Anna I. Kulpanovich, Marcelo de Bello Cioffi, Markus Stumm, Alla Frolova, Isabella Simonyan, Thomas Liehr, Samarth Bhatt, Monika Ziegler, Hasmik Mkrtchyan, Isolde Schreyer, Katharina Kreskowski, Thomas Martin, Ani Grigorian, Laura R. Rodríguez, Lukretija Brecevic, Evgenia Jaroshevich, Tatiana Egorova, Svetlana G. Vorsanova, Nadezda Kosyakova, Heike Nelle, Irina Naumchik, Natalia Shorokh, Anja Weise, Marina Manvelyan, Rouben Aroutiounian, Ali Sazci, Rolf-Dieter Wegner
Publikováno v:
Molecular Cytogenetics
Background Heterochromatic variants of pericentromere of chromosome 9 are reported and discussed since decades concerning their detailed structure and clinical meaning. However, detailed studies are scarce. Thus, here we provide the largest ever done
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b88e7e616715b34c4787c77d0df549f9
https://pubmed.ncbi.nlm.nih.gov/23547710
https://pubmed.ncbi.nlm.nih.gov/23547710
Autor:
Samarth Bhatt, A Polityko, Maria Isabel Melaragno, Roberta Santos Guilherme, Nadezda Kosyakova, Ahmed B. Hamid, Elisabeth Klein, Anna I. Kulpanovich, Claudia Venner, Thomas Liehr, Marianne Volleth
Publikováno v:
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology. 20(7)
Ring chromosomes and small supernumerary marker chromosomes (sSMC) are enigmatic types of derivative chromosomes, in which the telomeres are thought to play a crucial role in their formation and stabilization. Considering that there are only a few st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a575954be75e6a0bb38ff4a6d901d639
https://pubmed.ncbi.nlm.nih.gov/23076733
https://pubmed.ncbi.nlm.nih.gov/23076733
Autor:
Maria, Bucksch, Monika, Ziegler, Nadezda, Kosayakova, Milene V, Mulatinho, Milene V, Mulhatino, Juan C, Llerena, Susanne, Morlot, Wolfgang, Fischer, Anna D, Polityko, Anna I, Kulpanovich, Michael B, Petersen, Britta, Belitz, Vladimir, Trifonov, Anja, Weise, Thomas, Liehr, Ahmed B, Hamid
Publikováno v:
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society. 60(7)
A new multicolor fluorescence in situ hybridization (mFISH) probe set is presented, and its possible applications are highlighted in 25 clinical cases. The so-called heterochromatin-M-FISH (HCM-FISH) probe set enables a one-step characterization of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec5e94669cfd4df98a46425b9370c13d
https://pubmed.ncbi.nlm.nih.gov/22511603
https://pubmed.ncbi.nlm.nih.gov/22511603
Autor:
Anna D, Polityko, Olga M, Khurs, Anna I, Kulpanovich, Konstantin A, Mosse, Angelica V, Solntsava, Natalia V, Rumyantseva, Irina V, Naumchik, Thomas, Liehr, Anja, Weise, Hasmik, Mkrtchyan
Publikováno v:
European journal of medical genetics. 52(4)
An unusual mosaic karyotype was detected in a 6-year-old female patient with clinical diagnosis of Turner syndrome (TS). Cytogenetic and molecular cytogenetic studies revealed besides a cell line with 45,X a second cell line where the short arm of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fcb26d05f84fdae67c3d16e6406bfb8c
https://pubmed.ncbi.nlm.nih.gov/19375526
https://pubmed.ncbi.nlm.nih.gov/19375526