Zobrazeno 1 - 8
of 8
pro vyhledávání: '"E V, Baronova"'
Publikováno v:
Cytology and Genetics. 47:58-61
The results of a molecular cytogenetic study of the material of spontaneous abortions and nonprogressive pregnancies in the first trimester in 43 couples who were treated with various ART methods are presented in this paper. Chromosomal pathologies (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a3ee6887281ef5a58f7cc02e5c42eb2
https://doi.org/10.3103/s009545271301009x
https://doi.org/10.3103/s009545271301009x
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:
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::997873ae819f04dbab03033e145c952b
https://pubmed.ncbi.nlm.nih.gov/23427615
https://pubmed.ncbi.nlm.nih.gov/23427615
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ac9c82c21960d03f4d39a7da5590805d
https://pubmed.ncbi.nlm.nih.gov/18030726
https://pubmed.ncbi.nlm.nih.gov/18030726
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0f39e8ecb04ce9d0d8185949a322e177
https://pubmed.ncbi.nlm.nih.gov/16933854
https://pubmed.ncbi.nlm.nih.gov/16933854
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1dbd4d34dcaf3b05a312e12f8725fac0
https://pubmed.ncbi.nlm.nih.gov/16865993
https://pubmed.ncbi.nlm.nih.gov/16865993
Autor:
V V, Nastiukova, E V, Baronova
Publikováno v:
TSitologiia i genetika. 34(3)
The analysis of the cytogenetic anomalies frequencies in children with inborn defects of development was carried out, and the comparative evaluation of involving in cytogenetic anomalies of the individual chromosomes was determined. Chromosomes 9, 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::84d1737830e63cd5567189e1aaafe90c
https://pubmed.ncbi.nlm.nih.gov/10920861
https://pubmed.ncbi.nlm.nih.gov/10920861
Autor:
T E, Zerova, E V, Baronova, N G, Gorovenko, G N, Koblianskaia, T I, Buzhievskaia, S G, Vorsanova, Iu B, Iurov
Publikováno v:
TSitologiia i genetika. 29(5)
Four cases of patients with additional marker chromosomes are described. The clinical, cytogenetic and molecular cytogenetic methods have been used for investigation. The identification of marker chromosomes was made by using in situ hybridization an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0984acf254bb51ca5545795c0e68c7d0
https://pubmed.ncbi.nlm.nih.gov/8721845
https://pubmed.ncbi.nlm.nih.gov/8721845