Zobrazeno 1 - 6
of 6
pro vyhledávání: '"S K, Shandlorenko"'
Autor:
N V, Kovaleva, I V, Butomo, T N, Il'iashenko, I Iu, Vasil'eva, L E, Khitrikova, S K, Shandlorenko, M V, Prozorova
Publikováno v:
Tsitologiia. 44(11)
Among 1332 cases of trisomy 21 born within 1979-1999 in St. Petersburg, 76(5.7%) were carriers of a translocation between chromosome 21 and other acrocentrics. Among 43 Dq; 21q translocations, 17 were inherited from the mother, and one was inherited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d9056c83922f34fb98d6ee586191aa12
https://pubmed.ncbi.nlm.nih.gov/12561733
https://pubmed.ncbi.nlm.nih.gov/12561733
Autor:
N V, Kovaleva, I V, Butomo, D K, Verlinskaia, T N, Il'iashenko, I G, Pantova, M V, Prozorova, L E, Khitrikova, S K, Shandlorenko
Publikováno v:
Tsitologiia. 41(12)
These data have been collected from St. Petersburg Down Syndrome Register that comprises information on 1778 liveborn children with the Down syndrome, including three twin sets, ascertained within 1970-1996. Karyotypes were obtained in 1223 cases, of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::be494fbf9a5bda7a137b273396208824
https://pubmed.ncbi.nlm.nih.gov/10658271
https://pubmed.ncbi.nlm.nih.gov/10658271
Autor:
N V, Kovaleva, I V, Butomo, D K, Verlinskaia, D I, Mant, M N, Pavlova, I G, Pantova, M V, Prozorova, S K, Shandlorenko, I A, Shmatova
Publikováno v:
Genetika. 30(3)
Karyological study of 644 newborns with Down's syndrome (DS) revealed 37 translocation cases (5.7%). Translocations were inherited in 8 cases, in 17 cases they were sporadic, and in 12 cases parents were not examined. Total mutation rate per gamete p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::de125344dd75d7fc86675ac708fd4a70
https://pubmed.ncbi.nlm.nih.gov/8188060
https://pubmed.ncbi.nlm.nih.gov/8188060
Publikováno v:
Tsitologiia. 28(7)
Among 106 females with the Turner syndrome phenotype, two displayed rare chromosomal anomalies. In one patient, in addition to X-chromosome monosomy, among cultured lymphocytes cells with two isochromosomes made by long arms of X-chromosome were dete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e838558f3cdd0348a58e9b8f767858f4
https://pubmed.ncbi.nlm.nih.gov/3765110
https://pubmed.ncbi.nlm.nih.gov/3765110
Publikováno v:
Voprosy onkologii. 25(1)
The introduction in clinical practice of modern methods of cytogenetic assays offers new opportunities in studying the nature of leukemia. Up to date, however, no due attention was given to the recognition of chromosome disorders in patients with chr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b1c115bea5da021f17bc135ddf8e847
https://pubmed.ncbi.nlm.nih.gov/284662
https://pubmed.ncbi.nlm.nih.gov/284662
Publikováno v:
Pediatriia. (1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7d0d9fefe8c958027dddd436387c1ffc
https://pubmed.ncbi.nlm.nih.gov/432037
https://pubmed.ncbi.nlm.nih.gov/432037