Zobrazeno 1 - 10 of 40 pro vyhledávání: '"I V, Lur'e"'
1
[Translocation 11q;22q: a clinico-cytogenetic study]
Autor: I V, Lur'e, N V, Rumiantseva, L V, Podleshchuk, S I, Kozlova, V D, Kulak, I V, Naumchik, L B, Gorelik, T V, Zolotukhina, M I, Kuznetsov
Publikováno v: Genetika. 28(10)
Seven families with translocations t(11; 22) identified at our Institute and analysis of the literature showed that the imbalance resulted from such translocations is always due to nondisjunction 3:1. Nondisjunction occurs more often in the 1st meiot
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5aba75c91df96dd0928222d0b85984bb
https://pubmed.ncbi.nlm.nih.gov/1468637
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3
[Trisomy for distal segments of the long arm of chromosome 1]
Autor: I V, Lur'e, L A, Kodunov, N P, Veropotvelian, N V, Rumiantseva, D V, Zaletaev, M G, Belik
Publikováno v: Genetika. 25(12)
Clinical genetic analysis of distal trisomies 1q, based on the study of a t(1; 6) (q42.1; p24) family and the literature data, was performed. It was demonstrated that phenotypical manifestations of the trisomy are formed by nonspecific anomalies, due
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9eedc096b8b14a72e38309e72c3d0f24
https://pubmed.ncbi.nlm.nih.gov/2634579
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4
[Genetics of Patau's syndrome (an analysis of 59 families)]
Autor: G I, Laziuk, I V, Lur'e, D B, Gurevich
Publikováno v: TSitologiia i genetika. 18(6)
Different parental translocations were observed in 11 out of 59 families where a child with Patau's syndrome was born. All cases, except for one with t(13; 18) (q14; q23) in the father, revealed the Robertsonian translocations. In most cases there we
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a35a2189ea74978161471796d90b5928
https://pubmed.ncbi.nlm.nih.gov/6523569
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7
[Genetic syndromes of multiple congenital developmental defects]
Autor: G I, Laziuk, I V, Lur'e, E D, Cherstvoĭ
Publikováno v: Arkhiv patologii. 39(3)
Analysis of developmental defects in 615 children who had died in hospitals in Minsk during the 5-year period (1971--1975)showed that in 274 children defects were multiple. This number includes 78 children with chromosomal diseases and 37 children wi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8f6f251157147901cd9d387d19ee0dda
https://pubmed.ncbi.nlm.nih.gov/193472
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9
[Indications for amniocentesis for prenatal determination of fetal karyotype]
Autor: I V, Lur'e
Publikováno v: TSitologiia i genetika. 10(3)
Analysis of the data from 13 centres of prenatal diagnosis in different countries revealed that 35 out of 1532 pregnancies where diagnostical amniocentesis was performed terminated in "spontaneous" abortions. The frequency of "spontaneous" abortions
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ec4f31df60c6ab191041356896cbe529
https://pubmed.ncbi.nlm.nih.gov/1014080
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