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

189 related items for PubMed ID: 1083188

  • 1. [Trisomy 10q24--10qter].
    Dutrillaux B, Laurent C, Bernasconi S, Lejeune J.
    Ann Genet; 1975 Dec; 18(4):217-22. PubMed ID: 1083188
    [Abstract] [Full Text] [Related]

  • 2. The 12p trisomy syndrome.
    Armendares S, Salamanca F, Nava S, Ramirez S, Cantu JM.
    Ann Genet; 1975 Jun; 18(2):89-94. PubMed ID: 1081370
    [Abstract] [Full Text] [Related]

  • 3. [Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].
    Aledo AG, Gracia R, López Pajares I, González M, Oliver A, Peralta A.
    An Esp Pediatr; 1982 Aug; 17(2):125-9. PubMed ID: 7149479
    [Abstract] [Full Text] [Related]

  • 4. Further delineation of 7p trisomy. Case report and review of literature.
    Pallotta R, Dalprà L, Fusilli P, Zuffardi O.
    Ann Genet; 1996 Aug; 39(3):152-8. PubMed ID: 8839888
    [Abstract] [Full Text] [Related]

  • 5. [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].
    Rethoré MO, Larget-Piet L, Abonyi D, Boeswillwald M, Berger R, Carpentier S, Cruveiller J, Dutrillau B, Lafourcade J, Penneau M, Lejeune J.
    Ann Genet; 1970 Dec; 13(4):217-32. PubMed ID: 5313386
    [No Abstract] [Full Text] [Related]

  • 6. Distal 2q duplication: report of two familial cases and an attempt to define a syndrome.
    Zankl M, Schwanitz G, Schmid P, Zankl H, Dockter G, Rodewald A, Zang KD, Grosse KP.
    Am J Med Genet; 1979 Dec; 4(1):5-16. PubMed ID: 495653
    [Abstract] [Full Text] [Related]

  • 7. [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]

  • 8. [Cp trisomy: a new syndrome].
    Canu JM, Buentello L, Armendares S.
    Ann Genet; 1971 Sep; 14(3):177-86. PubMed ID: 5315464
    [No Abstract] [Full Text] [Related]

  • 9. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M, Hemly NA, Zaki MS.
    Genet Couns; 2007 Sep; 18(2):217-26. PubMed ID: 17710874
    [Abstract] [Full Text] [Related]

  • 10. Clinical features of monosomy 10qter.
    Zatterale A, Pagano L, Fioretti G, Caniglia M, Festa B, Renda S, Rinaldi MM, Ventruto V.
    Ann Genet; 1983 Sep; 26(2):106-8. PubMed ID: 6604483
    [Abstract] [Full Text] [Related]

  • 11. Partial trisomy 9 in the case of familial translocation 8/9 mat.
    Schwanitz G, Schamberger U, Rott HD, Wieczorek V.
    Ann Genet; 1974 Sep; 17(3):163-6. PubMed ID: 4548816
    [No Abstract] [Full Text] [Related]

  • 12. ["Free" 9p trisomy in a male child with severe mental retardation (author's transl)].
    Aller V, Abrisqueta JA, Martín-Lucas MA, de Torres ML, del Mazo J, Pérez-Castillo A.
    An Esp Pediatr; 1979 May; 12(5):463-8. PubMed ID: 464416
    [Abstract] [Full Text] [Related]

  • 13. Trisomy for the short arm of chromosome 10. Report of a new case resulting from segregation of a maternal balanced translocation t(10qter----q11::14p11----qter).
    Delaroche I, Bruni L, Giannotti A, Giampaolo R, Aebischer ML.
    Helv Paediatr Acta; 1984 May; 39(2):161-6. PubMed ID: 6543839
    [Abstract] [Full Text] [Related]

  • 14. The phenotypic and cytogenetic spectrum of partial trisomy 9.
    Wilson GN, Raj A, Baker D.
    Am J Med Genet; 1985 Feb; 20(2):277-82. PubMed ID: 3976721
    [Abstract] [Full Text] [Related]

  • 15. [Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case].
    Ayraud N, Galiana A, Llyod M, Deswarte M.
    Ann Genet; 1976 Mar; 19(1):65-8. PubMed ID: 1084126
    [Abstract] [Full Text] [Related]

  • 16. [Pure trisomy 9p 47,XX,+ del(9) (q11). Discovery of one cell 46,XX, del(9) (q11) in the father].
    Turleau C, De Grouchy J, Roubin M, Chavin-Colin F, Cachin O.
    Ann Genet; 1975 Jun; 18(2):125-9. PubMed ID: 1081365
    [Abstract] [Full Text] [Related]

  • 17. [7 cases of trisomy 2q34 leads to 2qter resulting from a familial t(2;8)(q34;23)].
    Laurent C, Biemont MC, Guibaud P, Guillot J, Noël B, Quack B, Geneviève M, Cressens ML.
    Ann Genet; 1978 Mar; 21(1):13-7. PubMed ID: 308338
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.
    Brisset S, Joly G, Ozilou C, Lapierre JM, Gosset P, LeLorc'h M, Raoul O, Turleau C, Vekemans M, Romana SP.
    Am J Med Genet; 2002 Dec 15; 113(4):339-45. PubMed ID: 12457405
    [Abstract] [Full Text] [Related]

  • 20. [9p trisomy syndrome. Two new cases (author's transl)].
    Martín Sánchez A, Delicado A, Izquierdo M, Oliver A, López Pajares I, Gracia R, Peralta A.
    An Esp Pediatr; 1981 May 15; 14(5):344-51. PubMed ID: 7294523
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.