These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

413 related items for PubMed ID: 6892078

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

  • 2. 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]

  • 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 Jun; 18(3):223-8. PubMed ID: 6235655
    [Abstract] [Full Text] [Related]

  • 4. [Familial observation of partial trisomy 6, and probable partial monosomy 18q by parental translocation].
    D'Emma C, Crippa L, Delozier C, Michail E, Graber P.
    J Genet Hum; 1982 Mar; 30(1):39-50. PubMed ID: 7130955
    [Abstract] [Full Text] [Related]

  • 5. [Two new cases of trisomy 10q21 to 10qter in two sisters due to paternal translocation t(9;10) (q34;q24)].
    Fraisse J, Lauras B, La Selve A, Freycon F.
    Ann Genet; 1977 Jun; 20(2):128-31. PubMed ID: 302687
    [Abstract] [Full Text] [Related]

  • 6. [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)].
    Raoul O, Rethoré MO, Dutriliaux B, Michon L, Lejeune J.
    Ann Genet; 1975 Mar; 18(1):35-9. PubMed ID: 1080036
    [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 Mar; 23(4):216-20. PubMed ID: 6971599
    [Abstract] [Full Text] [Related]

  • 8. 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 Mar; 11(4):355-61. PubMed ID: 11140413
    [Abstract] [Full Text] [Related]

  • 9. Cryptic subtelomeric translocation t(2;16)(q37;q24) segregating in a family with unexplained stillbirths and a dysmorphic, slightly retarded child.
    Giardino D, Finelli P, Gottardi G, Clerici D, Mosca F, Briscioli V, Larizza L.
    Eur J Hum Genet; 2001 Dec; 9(12):881-6. PubMed ID: 11840188
    [Abstract] [Full Text] [Related]

  • 10. [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 Dec; 28(3):149-53. PubMed ID: 3879147
    [Abstract] [Full Text] [Related]

  • 11. Partial trisomy 13 due to maternal translocation t(7;13)(p22q14).
    Martin-Lucas MA, Pérez-Castillo A, Abrisqueta JA, de Torres ML, Martin-Sempere MJ, Del Mazo J, Aller V.
    Ann Genet; 1982 Dec; 25(3):172-8. PubMed ID: 6982670
    [Abstract] [Full Text] [Related]

  • 12. Familial trisomy 11p resulting from a balanced paternal translocation: 3 new cases including first trimester diagnosis.
    Ogur G, Hayez F, Herinckx A, Van Regemorter N, Vamos E.
    J Genet Hum; 1988 Aug; 36(4):323-9. PubMed ID: 3221208
    [Abstract] [Full Text] [Related]

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

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.
    Wouters CH, van Bodegom TM, Moll HA, Govaerts LC.
    Ann Genet; 1999 Aug; 42(3):160-5. PubMed ID: 10526659
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Cytogenetic studies in reproductive loss.
    Schmidt R, Nitowsky HM, Dar H.
    JAMA; 1976 Jul 26; 236(4):369-73. PubMed ID: 947051
    [Abstract] [Full Text] [Related]

  • 19. Clinical and cytogenetic studies in a large (4;8) translocation family with pre- and postnatal Wolf syndrome.
    Tranebjaerg L, Petersen A, Hove K, Rehder H, Mikkelsen M.
    Ann Genet; 1984 Jul 26; 27(4):224-9. PubMed ID: 6335368
    [Abstract] [Full Text] [Related]

  • 20. De novo balanced translocation: 46, XX, t(13;20)(q34;p 11).
    Marinescu DD, Cioltei A, Pop T, Ioan D, Maximilian C.
    Endocrinologie; 1978 Jul 26; 16(4):295-8. PubMed ID: 734345
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 21.