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Journal Abstract Search

1044 related items for PubMed ID: 6235655

  • 1. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV, Prozorova MV, Khitrikova LE.
    Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655
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  • 4. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X.
    Panasiuk B, Usinskiené R, Kostyk E, Rybałko A, Stasiewicz-Jarocka B, Krzykwa B, Pieńkowska-Grela B, Kucinskas V, Michalova K, Midro AT.
    Ann Genet; 2004; 47(1):11-28. PubMed ID: 15050871
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  • 5. [Partial trisomy of chromosome 21 by maternal translocation t(15;21) (q26.2; q21)].
    Raoul O, Carpentier S, Dutrillaux B, Mallet R, Lejeune J.
    Ann Genet; 1976 Sep; 19(3):187-90. PubMed ID: 136225
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  • 7. [Double autosomal aberration: trisomy 21 and familial reciprocal translocation t(10;12)(p14;q21)].
    Butomo IV, Mashkova MV.
    Tsitologiia; 1977 Nov; 19(11):1291-6. PubMed ID: 146289
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  • 14. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
    Cetin Z, Mihci E, Keser I, Karaali K, Berker S, Luleci G.
    Genet Couns; 2012 Nov; 23(2):239-47. PubMed ID: 22876583
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  • 15. [Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)].
    Obry E, Piussan C, Risbourg B, Dutrillaux B.
    Ann Genet; 1980 Nov; 23(4):216-20. PubMed ID: 6971599
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  • 18. [Partial trisomy 13 for the distal long arm and its prenatal diagnosis].
    Zolotukhina TV, Rozovskiĭ IS, Bartseva OB, Vakhlamova IV, Bubnova NI.
    Genetika; 1982 Nov; 18(11):1899-905. PubMed ID: 6891355
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  • 19. [Frequency of chromosome variants in human populations].
    Kuleshov NP, Kulieva LM.
    Genetika; 1979 Nov; 15(3):745-51. PubMed ID: 160358
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