Zobrazeno 1 - 10
of 17
pro vyhledávání: '"L. V. Tavokina"'
Autor:
L. V. Popovych, A. V. Shatillo, N. B. Zelinska, L. V. Tavokina, O. V. Gorodna, G. B. Livshits, D. A. Sirokha, L. A. Livshits
Publikováno v:
Cytology and Genetics. 56:417-422
Publikováno v:
Biopolymers and Cell, Vol 32, Iss 1, Pp 49-53 (2016)
The presence of marker chromosomes in the human karyotype always requires a special diagnostic approach. Determination of the marker chromosome type and structure is of great diagnostic and prognostic importance. There are several methods of marker c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da41165fe692fb7f1ebee3bd7bafafab
http://dspace.nbuv.gov.ua/handle/123456789/152767
http://dspace.nbuv.gov.ua/handle/123456789/152767
Publikováno v:
Cytology and Genetics. 43:360-365
Data about some genetic factors of male infertility are presented, and methods, which may be used for its diagnosing, are studied. Among genetic factors the following are distinguished: changes in the level of genes (mutations), chromosomes (chromoso
Publikováno v:
TSitologiia i genetika. 47(1)
The results of molecular cytogenetic study of spontaneous abortions and material non progressive pregnancies in the first trimester in 43 couples who were treated with various methods of ART are presented in this report. Chromosomal pathology (CP) wa
Publikováno v:
TSitologiia i genetika. 43(5)
Data about some male infertility genetic factors is presented and methods that can be used for its diagnostics are considered. Among genetic factors changes of the genetic apparatus at gene level (mutations), chromosome level (chromosomal aberrations
Publikováno v:
TSitologiia i genetika. 41(4)
Results of cytogenetic and molecular-cytogenetic inspection of 210 matrimonial pairs with the problems of reproduction are presented. Different types of chromosomal aberrations have been detected in the karyotypes of the patients in 46 (10.95%) cases
Publikováno v:
TSitologiia i genetika. 40(6)
As a result of leadthrough 288 invasive manipulations with the use of cytogenetic and molecular-cytogenetic methods we have found 16 different disorders in the fetus karyotype of the expectant mothers of high risk groups. For the most part the Down s
Publikováno v:
TSitologiia i genetika. 40(3)
We present the prenatally identified case of mosaicism of chromosome 16 trisomy. A patient with the pregnancy complicated in the first trimester by the threat of breaking was refered to the high risk group according to the results of the screening pr
Publikováno v:
TSitologiia i genetika. 40(2)
It is known that the frequency of chromosomal abnormalities among spontaneous miscarriages of the first trimester of pregnancy makes 50-60%. Research of karyotypes of chorionic villus cells of miscarriages has been conducted by combining the standard
Autor:
L V, Tavokina, S G, Vorsanova, V D, Zukin, N I, Sopko, V M, Zinchenko, V V, Veselovskiĭ, A M, Bychkova, T V, Nikitchina, Iu B, Iurov
Publikováno v:
TSitologiia i genetika. 38(1)
Results of cytogenetic research of placental villi and amniotic fluid cells culture of the 22-weeks-old fetus with multiple congenital malformations (MCM) are presented. The absence of the short arm in one of the homologue of the chromosome 21 was re