Zobrazeno 1 - 10
of 18
pro vyhledávání: '"O A, Podugol'nikova"'
Autor:
O A, Podugol'nikova, V G, Solonichenko
Publikováno v:
TSitologiia i genetika. 28(3)
A significant reduction in the total amount of C heterochromatin of chromosomes 1, 9, 16, and Y was detected in six patients with Noonan's syndrome. The results obtained do not contradict the results of our previous investigations of the correlation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bc0afb0f9ff5ac1c313c2b42c90f7c7e
https://pubmed.ncbi.nlm.nih.gov/7974791
https://pubmed.ncbi.nlm.nih.gov/7974791
Publikováno v:
Tsitologiia. 19(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e4157af132b875ec77e51f601908602a
https://pubmed.ncbi.nlm.nih.gov/883026
https://pubmed.ncbi.nlm.nih.gov/883026
Publikováno v:
Tsitologiia. 16(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::82915bd1df1cf88cbe616fb55652ac07
https://pubmed.ncbi.nlm.nih.gov/4837559
https://pubmed.ncbi.nlm.nih.gov/4837559
Publikováno v:
Genetika. 20(1)
Polymorphism of the heterochromatic regions (HR) on chromosomes 1, 9, 16 and in three groups of boys at the age of 3 to 14 years was studied. Two groups of boys with olygophrenia of unknown etiology differed by the extent of mental defect, the latter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6efc7f5712dee429fa3b9960b9c63e08
https://pubmed.ncbi.nlm.nih.gov/6538157
https://pubmed.ncbi.nlm.nih.gov/6538157
Publikováno v:
Tsitologiia. 28(1)
The squares of Ag-stained nucleolar organizing regions of metaphase chromosomes have been estimated by scanning their negative images on the film and computer data processing. The intercellular variation of the sum of squares of nucleolar organizing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f16dcec4eec140a842affb1a5460b2e8
https://pubmed.ncbi.nlm.nih.gov/2420046
https://pubmed.ncbi.nlm.nih.gov/2420046
Autor:
O A, Podugol'nikova
Publikováno v:
TSitologiia i genetika. 21(5)
The inheritance of heterochromatic regions of chromosomes 1, 9, 16 and Y was studied in twelve families by means of measuring their C-segments. Maternal and paternal origin of chromosomes 1, 9 and 16 in the child was determined by two methods. The ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e4ecf572405d7b940aa9ff1ec0e0f03
https://pubmed.ncbi.nlm.nih.gov/2963417
https://pubmed.ncbi.nlm.nih.gov/2963417
Autor:
O A, Podugol'nikova
Publikováno v:
Tsitologiia. 29(6)
To test a hypothesis on potential role of large heterochromatic regions in chromosome nondisjunction polymorphism of C segments of chromosomes 1, 9, and 16 in 70 children with Down's syndrome were examined. The C segment lengths of the above chromoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::65861730d3d644a11aaca45424242a81
https://pubmed.ncbi.nlm.nih.gov/2957841
https://pubmed.ncbi.nlm.nih.gov/2957841
Publikováno v:
Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952). 82(3)
Pathogenetic examinations of 96 mentally retarded children with multiple somatic anomalies and developmental defects (but without Down's disease) were carried out. Changes of the caryotype were discovered in 36 children (37.5%). In 21 children (22.0%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d061a1190b99db9704b642375a7ce4d1
https://pubmed.ncbi.nlm.nih.gov/7080777
https://pubmed.ncbi.nlm.nih.gov/7080777
Autor:
O A, Podugol'nikova, A P, Korostelev
Publikováno v:
Tsitologiia. 16(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9b0eb2d555cc695eef978c1fecde6c35
https://pubmed.ncbi.nlm.nih.gov/4420838
https://pubmed.ncbi.nlm.nih.gov/4420838
Publikováno v:
Genetika. 17(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df9d2d4258870881f23c5f5dadddd74c
https://pubmed.ncbi.nlm.nih.gov/7194840
https://pubmed.ncbi.nlm.nih.gov/7194840