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Journal Abstract Search

537 related items for PubMed ID: 6607704

  • 1. "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]

  • 2. [Phenotypic disorders in balanced reciprocal translocation: karyotype 46,XY,rcp(13; 21)(q22; q22)].
    Badalian LO, Malygina NA, Gozman TV, Petrukhin AS, Mutovin GR.
    Tsitol Genet; 1982; 16(2):17-21. PubMed ID: 7101445
    [Abstract] [Full Text] [Related]

  • 3. [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]

  • 4. [Reciprocal syndromes caused by deficiency duplication resulting from maternal t(10;18)(p12;q22) translocation].
    Rethoré MO, Prieur M, de Blois MC, Naffah J, Ravel A, Villain E, Lejeune J.
    Ann Genet; 1985; 28(3):149-53. PubMed ID: 3879147
    [Abstract] [Full Text] [Related]

  • 5. [Trisomy 12(pter----q12) and monosomy 21(pter----q21). A propos of a case].
    Arnaud M, Bourrouillou G, Sablayrolles B, Rolland M, Dutau G, Colombies P, Rochiccioli P.
    J Genet Hum; 1984 Dec; 32(5):369-75. PubMed ID: 6527133
    [Abstract] [Full Text] [Related]

  • 6. Brief clinical report: dup(4p15 leads to 4pter) in a 19-year-old woman resulting from a maternal 4;14 translocation.
    Clark CE, Telfer MA, Cowell HR, Kalamchi A, Steg NL.
    Am J Med Genet; 1982 Jan; 11(1):37-42. PubMed ID: 7065001
    [Abstract] [Full Text] [Related]

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

  • 8. Elucidation of the cytogenetic abnormality in a 4p- "phenocopy".
    Curry CJ, Ying KL, O'Lague P, Tsai J.
    Birth Defects Orig Artic Ser; 1982 Jan; 18(3B):275-86. PubMed ID: 7139110
    [No Abstract] [Full Text] [Related]

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

  • 10. Two reciprocal translocations t(9p+;13q-) and t(13q-;21q+): a study of the families.
    Prieto F, Badia L, Asensi F, Roques V.
    Hum Genet; 1980 Jan; 54(1):7-11. PubMed ID: 7390483
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Balanced rearrangement of chromosomes 2, 5, and 13 in a family with duplication 5q and fetal loss.
    Evans MI, White BJ, Kent SG, Levine MA, Levin SW, Larsen JW.
    Am J Med Genet; 1984 Dec; 19(4):783-90. PubMed ID: 6517101
    [Abstract] [Full Text] [Related]

  • 13. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
    Ito M, Mutoh K, Okuno T, Mikawa H, Edagawa J, Abe T.
    Ann Genet; 1983 Dec; 26(2):116-9. PubMed ID: 6604486
    [Abstract] [Full Text] [Related]

  • 14. Wolf-Hirschhorn syndrome owing to 1:3 segregation of a maternal 4;21 translocation.
    Bauer K, Howard-Peebles PN, Keele D, Friedman JM.
    Am J Med Genet; 1985 Jun; 21(2):351-6. PubMed ID: 4014316
    [Abstract] [Full Text] [Related]

  • 15. De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21.
    Riegel M, Baumer A, Piram A, Ortolan D, Peres LC, Pina-Neto JM.
    Genet Couns; 2001 Jun; 12(1):69-75. PubMed ID: 11332980
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Partial duplication 5q syndrome: phenotypic similarity in two sisters with identical karyotype (partial duplication 5q33 leads to 5qter and partial deficiency 8p23 leads to pter).
    Bartsch-Sandhoff M, Liersch R.
    Ann Genet; 1977 Dec; 20(4):281-4. PubMed ID: 305758
    [Abstract] [Full Text] [Related]

  • 18. Distal trisomy 14q due to tandem duplication (q24 leads to q32).
    Orye E, Van Bever H, Desimpel H.
    Ann Genet; 1983 Dec; 26(4):238-9. PubMed ID: 6607705
    [Abstract] [Full Text] [Related]

  • 19. [Translocation t (13:21) (q22:q22) in mother and monosomia 21 and partial trisomy 13 on her son (author's transl)].
    Prieto García F, Badía Garrabou L, Ferrer Calvette J.
    An Esp Pediatr; 1977 Dec; 10(12):927-32. PubMed ID: 607844
    [Abstract] [Full Text] [Related]

  • 20. [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]

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