Zobrazeno 1 - 3
of 3
pro vyhledávání: '"L. Y. Lozynska"'
Publikováno v:
Біологічні студії, Vol 8, Iss 1, Pp 45-52 (2014)
The clinical examination, genealogical and molecular genetic analysis of the probands and the risk group of three families with Peutz–Jeghers syndrome were carried out. The mutations of STK11 gene in exons 1, 2, 3 and 4, that lead to the formation
Externí odkaz:
https://doaj.org/article/c0d4ac366fc2439abc37cab86b4e0af4
Autor:
L Y, Lozynska, A, Plawski, M R, Lozynska, I, Vytvytskyi, R Y, Lozynskyi, N, Prokopchuk, B, Tretiak
Publikováno v:
Experimental oncology. 40(1)
To study the relationship between the genotype and the phenotype in the patients with Hermansky - Pudlak syndrome (HPS) associated with granulomatous colitis; to monitor clinical course of the disease for adequate treatment, cancer surveillance and g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::407a34cb8dc39e020a930cf7c6be1684
https://pubmed.ncbi.nlm.nih.gov/29600982
https://pubmed.ncbi.nlm.nih.gov/29600982
Autor:
B Tretiak, L. Y. Lozynska, M. R. Lozynska, I. K. Vytvytskyi, R Y Lozynskyi, A. Plawski, N. M. Prokopchuk
Publikováno v:
Scopus-Elsevier
Aim: To study the relationship between the genotype and the phenotype in the patients with Hermansky — Pudlak syndrome (HPS) associated with granulomatous colitis; to monitor clinical course of the disease for adequate treatment, cancer surveillanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e635240262a97207c278660ba66a6130
http://dspace.nbuv.gov.ua/handle/123456789/139244
http://dspace.nbuv.gov.ua/handle/123456789/139244
