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Journal Abstract Search

1232 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
    [Abstract] [Full Text] [Related]

  • 2. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22).
    Rivera H, Rivas F, Plascencia L, Cantú JM.
    Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704
    [Abstract] [Full Text] [Related]

  • 3. A boy with trisomic Down's syndrome and a familial 5-?7 translocation, 47,XY,+21, t (5q-; ?7p+).
    Yanagisawa S.
    Jinrui Idengaku Zasshi; 1972 Sep; 17(1):38-43. PubMed ID: 4265909
    [No Abstract] [Full Text] [Related]

  • 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 Sep; 47(1):11-28. PubMed ID: 15050871
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 6. Unusual chromosome aberrations in 3 children with Down syndrome.
    Osztovics M, Tóth S, Wilhelm O.
    Acta Paediatr Acad Sci Hung; 1982 Sep; 23(3):283-9. PubMed ID: 6217717
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 8. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
    Cohen MM, Ornoy A, Rosenmann A, Kohn G.
    Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372
    [Abstract] [Full Text] [Related]

  • 9. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B, Hacihanefioglu S, Silahtaroglu A, Yilmaz S, Deviren A, Cenani A.
    Genet Couns; 2000 Jun; 11(4):355-61. PubMed ID: 11140413
    [Abstract] [Full Text] [Related]

  • 10. Three interesting cases of Down's syndrome.
    Pérez-Castillo A, Del Mazo J, Abrisqueta JA.
    Ann Genet; 1983 Jun; 26(2):123-8. PubMed ID: 6225371
    [Abstract] [Full Text] [Related]

  • 11. Proximal 14 trisomy 46,XX, -22 +der(14)t(14;22) (q21;q11)mat.
    Fried K, Goldberg MD, Rosenblatt M.
    Teratology; 1980 Jun; 21(3):309-12. PubMed ID: 7455919
    [No Abstract] [Full Text] [Related]

  • 12. [Familial pericentric inversion of y chromosome and Down's syndrome].
    García Sagredo JM, Morán Cabré A, San Román Cos-Gayón C.
    An Esp Pediatr; 1975 Jun; 8(1):68-71. PubMed ID: 123717
    [Abstract] [Full Text] [Related]

  • 13. An infant with trisomy 9pter yields 9q22 resulting from 3:1 segregation in a 46,XX t(1;9) (p36;q22) mother.
    Neu RL, Dennis NR, Lanman JT, Bannerman RM.
    Ann Genet; 1979 Jun; 22(3):151-4. PubMed ID: 316670
    [Abstract] [Full Text] [Related]

  • 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 Jun; 23(2):239-47. PubMed ID: 22876583
    [Abstract] [Full Text] [Related]

  • 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 Jun; 23(4):216-20. PubMed ID: 6971599
    [Abstract] [Full Text] [Related]

  • 16. Translocation (14;21)(q11;q22) in a woman with history of abortions and a child with Down's syndrome.
    Sudha T, Gopinath PM.
    Ann Genet; 1990 Jun; 33(3):162-4. PubMed ID: 2149630
    [Abstract] [Full Text] [Related]

  • 17. [Human chromosome polymorphism and disordered reproductive function. II. C-variant chromosomes].
    Tsvetkova TG, Iankova MF.
    Genetika; 1979 Jun; 15(10):1870-9. PubMed ID: 91543
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 19. [Frequency of chromosome variants in human populations].
    Kuleshov NP, Kulieva LM.
    Genetika; 1979 Nov; 15(3):745-51. PubMed ID: 160358
    [Abstract] [Full Text] [Related]

  • 20. [Familial balanced chromosome translocation t(12;13) in a family with several deformed stillbirths].
    Bommer C, Körner H.
    Zentralbl Gynakol; 1982 Nov; 104(24):1578-83. PubMed ID: 6892078
    [Abstract] [Full Text] [Related]

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