Zobrazeno 1 - 7
of 7
pro vyhledávání: '"N I, Voskoboĭnik"'
Publikováno v:
Arkhiv patologii. 56(2)
Silver staining was used to investigate transcription activity of ribosomal genes of leukemia granulocytes in the interphase in 32 patients with PA-positive chronic myeloid leukemia (CML) and 26 healthy subjects. Visual calculation of nucleolar argen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df135223726eab42bce3b2a5367dd7dd
https://pubmed.ncbi.nlm.nih.gov/8037588
https://pubmed.ncbi.nlm.nih.gov/8037588
Publikováno v:
Genetika. 29(3)
Comparative analysis of transcriptional activity of human nucleolus organizer regions (NOR) of the chromosomes in the group of the control phenotypically healthy individuals (I) and in the spouses with repeated spontaneous abortions (II) was conducte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3c3882a8f6c942697b603a624e18e358
https://pubmed.ncbi.nlm.nih.gov/8486271
https://pubmed.ncbi.nlm.nih.gov/8486271
Publikováno v:
Genetika. 29(2)
Relationship between the data on hybridization of the cloned sequences of the satellite DNA III located in the short arm of the acrocentric chromosomes and the hybridization data on the cloned fragments of 28S and 18S rRNA genes, as well as the trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d32f52417b4ef53d8fe33ff843d83b2
https://pubmed.ncbi.nlm.nih.gov/8486251
https://pubmed.ncbi.nlm.nih.gov/8486251
Publikováno v:
TSitologiia i genetika. 18(3)
A cytogenetic study was carried out in the chromosome set for 202 couples with recurrent spontaneous abortions of unknown genesis. Anomalies in the chromosome set were observed in 2.5% of cases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dd9506e5f8ce8ea740ff535627a6a35c
https://pubmed.ncbi.nlm.nih.gov/6464193
https://pubmed.ncbi.nlm.nih.gov/6464193
Publikováno v:
TSitologiia i genetika. 15(2)
Primary amenorrhea was studied in 64 women. Chromosome abnormalities or karyotype-phenotype non-conformity were found in 31 of 64 patients (48.4%). The following types of chromosomal pathology were found out: 7 cases with 45,X constitution; 3--45,X/4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4a4440febd225a3b7ee63159889a33f1
https://pubmed.ncbi.nlm.nih.gov/7233555
https://pubmed.ncbi.nlm.nih.gov/7233555
Publikováno v:
Genetika. 25(8)
The frequency and average amount of copy number per genome were defined for standard and a number of new variants of BamHI 5'-NTS RFLP from populations of Moscow, Riga and individuals with Down syndrome. It was demonstrated that the populations studi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3dd65b37635861ea87528441117a6817
https://pubmed.ncbi.nlm.nih.gov/2573559
https://pubmed.ncbi.nlm.nih.gov/2573559
Publikováno v:
Genetika. 23(3)
A comparative analysis of structural variability of C-bands on chromosomes 1, 9, 16 and Y was conducted in 50 phenotypically normal adults and 25 couples with repeated spontaneous abortions. Reduction of both the total amount of heterochromatin in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8c2c87daa58dc928cff6cab636e41450
https://pubmed.ncbi.nlm.nih.gov/3569898
https://pubmed.ncbi.nlm.nih.gov/3569898